ESTROPIPATE - estropipate tablet 
Barr Laboratories Inc.

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ESTROPIPATE TABLETS, USP

Revised SEPTEMBER 2002

21007270102

Rx only

(Three Patient Information Leaflets Enclosed - Tear at Perforation)

Description:

Estropipate, (formerly piperazine estrone sulfate), is a natural estrogenic substance prepared from purified crystalline estrone, solubilized as the sulfate and stabilized with piperazine. It is appreciably soluble in water and has almost no odor or taste - properties which are ideally suited for oral administration. The amount of piperazine in Estropipate Tablets is not sufficient to exert a pharmacological action. Its addition ensures solubility, stability, and uniform potency of the estrone sulfate. Chemically estropipate is represented by estra-1,3,5(10)-trien-17-one, 3-(sulfooxy)-, compound with piperazine (1:1). The structural formula may be represented as follows:

Estropipate Tablets are available for oral administration containing 0.75 mg, 1.5 mg or 3 mg estropipate (calculated as sodium estrone sulfate 0.625 mg, 1.25 mg and 2.5 mg, respectively).

Inactive Ingredients: Colloidal silicon dioxide, crospovidone, lactose monohydrate, magnesium stearate, and pregelatinized starch. The 0.75 mg also contains D&C yellow no. 10 aluminum lake and FD&C yellow no. 6 aluminum lake. The 1.5 mg also contains FD&C yellow no. 6 aluminum lake. The 3 mg also contains FD&C blue no. 2 aluminum lake.

Clinical Pharmacology:

Estrogen drug products act by regulating the transcription of a limited number of genes. Estrogens diffuse through cell membranes, distribute themselves throughout the cell, and bind to and activate the nuclear estrogen receptor, a DNA-binding protein which is found in estrogen-responsive tissues. The activated estrogen receptor binds to specific DNA sequences, or hormone-response elements, which enhance the transcription of adjacent genes and in turn lead to the observed effects. Estrogen receptors have been identified in tissues of the reproductive tract, breast, pituitary, hypothalamus, liver, and bone of women.

Estrogens are important in the development and maintenance of the female reproductive system and secondary sex characteristics. By a direct action, they cause growth and development of the uterus, Fallopian tubes, and vagina. With other hormones, such as pituitary hormones and progesterone, they cause enlargement of the breasts through promotion of ductal growth, stromal development, and the accretion of fat. Estrogens are intricately involved with other hormones, especially progesterone, in the processes of the ovulatory menstrual cycle and pregnancy, and affect the release of pituitary gonadotropins. They also contribute to the shaping of the skeleton, maintenance of tone and elasticity of urogenital structures, changes in the epiphyses of the long bones that allow for the pubertal growth spurt and its termination, and pigmentation of the nipples and genitals.

Estrogens occur naturally in several forms. The primary source of estrogen in normally cycling adult women is the ovarian follicle, which secretes 70 to 500 micrograms of estradiol daily, depending on the phase of the menstrual cycle. This is converted primarily to estrone, which circulates in roughly equal proportion to estradiol, and to small amounts of estriol. After menopause, most endogenous estrogen is produced by conversion of androstenedione, secreted by the adrenal cortex, to estrone by peripheral tissues. Thus, estrone—especially in its sulfate ester form—is the most abundant circulating estrogen in postmenopausal women. Although circulating estrogens exist in a dynamic equilibrium of metabolic interconversions, estradiol is the principal intracellular human estrogen and is substantially more potent than estrone or estriol at the receptor.

Estrogens used in therapy are well absorbed through the skin, mucous membranes, and gastrointestinal tract. When applied for a local action, absorption is usually sufficient to cause systemic effects. When conjugated with aryl and alkyl groups for parenteral administration, the rate of absorption of oily preparations is slowed with a prolonged duration of action, such that a single intramuscular injection of estradiol valerate or estradiol cypionate is absorbed over several weeks.

Administered estrogens and their esters are handled within the body essentially the same as the endogenous hormones. Metabolic conversion of estrogens occurs primarily in the liver (first pass effect), but also at local target tissue sites. Complex metabolic processes result in a dynamic equilibrium of circulating conjugated and unconjugated estrogenic forms which are continually interconverted, especially between estrone and estradiol and between esterified and non-esterified forms. Although naturally-occurring estrogens circulate in the blood largely bound to sex hormone-binding globulin and albumin, only unbound estrogens enter target tissue cells. A significant proportion of the circulating estrogen exists as sulfate conjugates, especially estrone sulfate, which serves as a circulating reservoir for the formation of more active estrogenic species. A certain proportion of the estrogen is excreted into the bile and then reabsorbed from the intestine. During this enterohepatic recirculation, estrogens are desulfated and resulfated and undergo degradation through conversion to less active estrogens (estriol and other estrogens), oxidation to nonestrogenic substances (catecholestrogens, which interact with catecholamine metabolism, especially in the central nervous system), and conjugation with glucuronic acids (which are then rapidly excreted in the urine).

When given orally, naturally-occurring estrogens and their esters are extensively metabolized (first pass effect) and circulate primarily as estrone sulfate, with smaller amounts of other conjugated and unconjugated estrogenic species. This results in limited oral potency. By contrast, synthetic estrogens, such as ethinyl estradiol and the nonsteroidal estrogens, are degraded very slowly in the liver and other tissues, which results in their high intrinsic potency. Estrogen drug products administered by non-oral routes are not subject to first-pass metabolism, but also undergo significant hepatic uptake, metabolism, and enterohepatic recycling.

Indications and Usage:

Estropipate tablets are indicated in the:

1. Treatment of moderate to severe vasomotor symptoms associated with menopause. There is no adequate evidence that estrogens are effective for nervous symptoms or depression which might occur during menopause and they should not be used to treat these conditions.
2. Treatment of vulval and vaginal atrophy.
3. Treatment of hypoestrogenism due to hypogonadism, castration or primary ovarian failure.
4. Prevention of osteoporosis.

Since estrogen administration is associated with risk, selection of patients should ideally be based on prospective identification of risk factors for developing osteoporosis. Unfortunately, there is no certain way to identify those women who will develop osteoporotic fractures. Most prospective studies of efficacy for this indication have been carried out in white menopausal women, without stratification by other risk factors, and tend to show a universally salutary effect on bone. Thus, patient selection must be individualized based on the balance of risks and benefits. A more favorable risk/benefit ratio exists in a hysterectomized woman because she has no risk of endometrial cancer (see Boxed WARNINGS).

Estrogen replacement therapy reduces bone resorption and retards or halts postmenopausal bone loss. Case-control studies have shown an approximately 60 percent reduction in hip and wrist fractures in women whose estrogen replacement was begun within a few years of menopause. Studies also suggest that estrogen reduces the rate of vertebral fractures. Even when started as late as 6 years after menopause, estrogen prevents further loss of bone mass for as long as the treatment is continued. The results of a double-blind, placebo-controlled two-year study have shown that treatment with one tablet of estropipate 0.75 mg daily for 25 days (of a 31-day cycle per month) prevents vertebral bone mass loss in postmenopausal women. When estrogen therapy is discontinued, bone mass declines at a rate comparable to the immediate postmenopausal period. There is no evidence that estrogen replacement therapy restores bone mass to premenopausal levels.

At skeletal maturity there are sex and race differences in both the total amount of bone present and its density, in favor of men and blacks. Thus, women are at higher risk than men because they start with less bone mass and, for several years following natural or induced menopause, the rate of bone mass decline is accelerated. White and Asian women are at higher risk than black women.

Early menopause is one of the strongest predictors for the development of osteoporosis. In addition, other factors affecting the skeleton which are associated with osteoporosis include genetic factors (small build, family history), endocrine factors (nulliparity, thyrotoxicosis, hyperparathyroidism, Cushing’s syndrome, hyperprolactinemia, Type I diabetes), lifestyle (cigarette smoking, alcohol abuse, sedentary exercise habits) and nutrition (below average body weight, dietary calcium intake).

The mainstays of prevention and management of osteoporosis are estrogen, an adequate lifetime calcium intake, and exercise. Postmenopausal women absorb dietary calcium less efficiently than premenopausal women and require an average of 1500 mg/day of elemental calcium to remain in neutral calcium balance. By comparison, premenopausal women require about 1000 mg/day and the average calcium intake in the USA is 400-600 mg/day. Therefore, when not contraindicated, calcium supplementation may be helpful.

Weight-bearing exercise and nutrition may be important adjuncts to the prevention and management of osteoporosis. Immobilization and prolonged bed rest produce rapid bone loss, while weight-bearing exercise has been shown both to reduce bone loss and to increase bone mass. The optimal type and amount of physical activity that would prevent osteoporosis have not been established, however in two studies an hour of walking and running exercises twice or three times weekly significantly increased lumbar spine bone mass.

Contraindications:

Estrogens should not be used in individuals with any of the following conditions:

1. Known or suspected pregnancy (see Boxed WARNINGS). Estrogens may cause fetal harm when administered to a pregnant woman.
2. Undiagnosed abnormal genital bleeding.
3. Known or suspected cancer of the breast except in appropriately selected patients being treated for metastatic disease.
4. Known or suspected estrogen-dependent neoplasia.
5. Active thrombophlebitis or thromboembolic disorders.

Warnings:

Induction of Malignant Neoplasms:

Endometrial Cancer:

The reported endometrial cancer risk among unopposed estrogen users is about 2 to 12 fold greater than in non-users, and appears dependent on duration of treatment and on estrogen dose. Most studies show no significant increased risk associated with use of estrogens for less than one year. The greatest risk appears associated with prolonged use—with increased risks of 15 to 24-fold for five to ten years or more. In three studies, persistence of risk was demonstrated for 8 to over 15 years after cessation of estrogen treatment. In one study a significant decrease in the incidence of endometrial cancer occurred six months after estrogen withdrawal. Concurrent progestin therapy may offset this risk but the overall health impact in postmenopausal women is not known (see PRECAUTIONS).

Breast Cancer:

While the majority of studies have not shown an increased risk of breast cancer in women who have ever used estrogen replacement therapy, some have reported a moderately increased risk (relative risks of 1.3 - 2.0) in those taking higher doses or those taking lower doses for prolonged periods of time, especially in excess of 10 years. Other studies have not shown this relationship.

Congenital Lesions with Malignant Potential:

Estrogen therapy during pregnancy is associated with an increased risk of fetal congenital reproductive tract disorders, and possibly other birth defects. Studies of women who received DES during pregnancy have shown that female offspring have an increased risk of vaginal adenosis, squamous cell dysplasia of the uterine cervix, and clear cell vaginal cancer later in life; male offspring have an increased risk of urogenital abnormalities and possibly testicular cancer later in life. Although some of these changes are benign, others are precursors of malignancy.

Gallbladder Disease:

Two studies have reported a 2- to 4-fold increase in the risk of gallbladder disease requiring surgery in women receiving postmenopausal estrogens.

Cardiovascular Disease:

Large doses of estrogen (5 mg conjugated estrogens per day), comparable to those used to treat cancer of the prostate and breast, have been shown in a large prospective clinical trial in men to increase the risks of nonfatal myocardial infarction, pulmonary embolism, and thrombophlebitis. These risks cannot necessarily be extrapolated from men to women. However, to avoid the theoretical cardiovascular risk to women caused by high estrogen doses, the dose for estrogen replacement therapy should not exceed the lowest effective dose.

Elevated blood pressure:

Occasional blood pressure increases during estrogen replacement therapy have been attributed to idiosyncratic reactions to estrogens. More often, blood pressure has remained the same or has dropped. One study showed that postmenopausal estrogen users have higher blood pressure than nonusers. Two other studies showed slightly lower blood pressure among estrogen users compared to nonusers. Postmenopausal estrogen use does not increase the risk of stroke. Nonetheless, blood pressure should be monitored at regular intervals with estrogen use.

Hypercalcemia:

Administration of estrogens may lead to severe hypercalcemia in patients with breast cancer and bone metastases. If this occurs, the drug should be stopped and appropriate measures taken to reduce the serum calcium level.

Precautions:

General:

Addition of a Progestin:

Studies of the addition of a progestin for ten or more days of a cycle of estrogen administration have reported a lowered incidence of endometrial hyperplasia than would be induced by estrogen treatment alone. Morphological and biochemical studies of endometria suggest that 10 to 14 days of progestin are needed to provide maximal maturation of the endometrium and to reduce the likelihood of hyperplastic changes.

There are, however, possible risks which may be associated with the use of progestins in estrogen replacement regimens. These include: (1) adverse effects on lipoprotein metabolism (lowering HDL and raising LDL) which could diminish the purported cardioprotective effect of estrogen therapy (see PRECAUTIONS below); (2) impairment of glucose tolerance; and (3) possible enhancement of mitotic activity in breast epithelial tissue, although few epidemiological data are available to address this point (see PRECAUTIONS below).

The choice of progestin, its dose, and its regimen may be important in minimizing these adverse effects, but these issues remain to be clarified.

Cardiovascular Risk:

A causal relationship between estrogen replacement therapy and reduction of cardiovascular disease in postmenopausal women has not been proven. Furthermore, the effect of added progestins on this putative benefit is not yet known.

In recent years many published studies have suggested that there may be a cause-effect relationship between postmenopausal oral estrogen replacement therapy without added progestins and a decrease in cardiovascular disease in women. Although most of the observational studies which assessed this statistical association have reported a 20% to 50% reduction in coronary heart disease risk and associated mortality in estrogen takers, the following should be considered when interpreting these reports:

(1) Because only one of these studies was randomized and it was too small to yield statistically significant results, all relevant studies were subject to selection bias. Thus, the apparently reduced risk of coronary artery disease cannot be attributed with certainty to estrogen replacement therapy. It may instead have been caused by life-style and medical characteristics of the women studied with the result that healthier women were selected for estrogen therapy. In general, treated women were of higher socioeconomic and educational status, more slender, more physically active, more likely to have undergone surgical menopause, and less likely to have diabetes than the untreated women. Although some studies attempted to control for these selection factors, it is common for properly designed randomized trials to fail to confirm benefits suggested by less rigorous study designs. Thus, ongoing and future large-scale randomized trials may fail to confirm this apparent benefit.

(2) Current medical practice often includes the use of concomitant progestin therapy in women with intact uteri (see PRECAUTIONS and WARNINGS). While the effects of added progestins on the risk of ischemic heart disease are not known, all available progestins reverse at least some of the favorable effects of estrogens on HDL and LDL levels.

(3) While the effects of added progestins on the risk of breast cancer are also unknown, available epidemiological evidence suggests that progestins do not reduce, and may enhance, the moderately increased breast cancer incidence that has been reported with prolonged estrogen replacement therapy (see WARNINGS above).

Because relatively long-term use of estrogens by a woman with a uterus has been shown to induce endometrial cancer, physicians often recommend that women who are deemed candidates for hormone replacement should take progestins as well as estrogens. When considering prescribing concomitant estrogens and progestins for hormone replacement therapy, physicians and patients are advised to carefully weigh the potential benefits and risks of the added progestin. Large-scale randomized, placebo-controlled, prospective clinical trials are required to clarify these issues.

Physical Examination:

A complete medical and family history should be taken prior to the initiation of any estrogen therapy. The pretreatment and periodic physical examinations should include special reference to blood pressure, breasts, abdomen, and pelvic organs, and should include a Papanicolaou smear. As a general rule, estrogen should not be prescribed for longer than one year without reexamining the patient.

Hypercoagulability:

Some studies have shown that women taking estrogen replacement therapy have hypercoagulability, primarily related to decreased antithrombin activity. This effect appears dose- and duration-dependent and is less pronounced than that associated with oral contraceptive use. Also, postmenopausal women tend to have increased coagulation parameters at baseline compared to premenopausal women. There is some suggestion that low dose postmenopausal mestranol may increase the risk of thromboembolism, although the majority of studies (of primarily conjugated estrogens users) report no such increase. There is insufficient information on hypercoagulability in women who have had previous thromboembolic disease.

Familial Hyperlipoproteinemia:

Estrogen therapy may be associated with massive elevations of plasma triglycerides leading to pancreatitis and other complications in patients with familial defects of lipoprotein metabolism.

Fluid Retention:

Because estrogens may cause some degree of fluid retention, conditions which might be exacerbated by this factor, such as asthma, epilepsy, migraine, and cardiac or renal dysfunction, require careful observation.

Uterine Bleeding and Mastodynia:

Certain patients may develop undesirable manifestations of estrogenic stimulation, such as abnormal uterine bleeding and mastodynia.

Impaired Liver Function:

Estrogens may be poorly metabolized in patients with impaired liver function and should be administered with caution.

Information for the patient:

See text of Patient Package Leaflet below.

Laboratory Tests:

Estrogen administration should generally be guided by clinical response at the smallest dose, rather than laboratory monitoring, for relief of symptoms for those indications in which symptoms are observable. For prevention and treatment of osteoporosis, however, see DOSAGE AND ADMINISTRATION section.

Drug/Laboratory Test Interactions:

Accelerated prothrombin time, partial thromboplastin time, and platelet aggregation time; increased platelet count; increased factors II, VII antigen, VIII antigen, VIII coagulant activity, IX, X, XII, VII-X complex, II-VII-X complex, and beta-thromboglobulin; decreased levels of anti-factor Xa and antithrombin III, decreased antithrombin III activity; increased levels of fibrinogen and fibrinogen activity; increased plasminogen antigen and activity.

Increased thyroid-binding globulin (TBG) leading to increased circulating total thyroid hormone, as measured by protein-bound iodine (PBI), T4 levels (by column or by radioimmunoassay) or T3 levels by radioimmunoassay. T3 resin uptake is decreased, reflecting the elevated TBG. Free T4 and free T3 concentrations are unaltered.

Other binding proteins may be elevated in serum, i.e., corticosteroid binding globulin (CBG), sex hormone-binding globulin (SHBG), leading to increased circulating corticosteroids and sex steroids respectively. Free or biologically active hormone concentrations are unchanged. Other plasma proteins may be increased (angiotensinogen/renin substrate, alpha-1-antitrypsin, ceruloplasmin).

Increased plasma HDL and HDL-2 subfraction concentrations, reduced LDL cholesterol concentration, increased triglycerides levels.

Impaired glucose tolerance.

Reduced response to metyrapone test.

Reduced serum folate concentration.

Carcinogenesis, Mutagenesis, Impairment of Fertility:

Long term continuous administration of natural and synthetic estrogens in certain animal species increases the frequency of carcinomas of the breast, uterus, cervix, vagina, testis, and liver. See CONTRAINDICATIONS and WARNINGS.

Pregnancy:

Teratogenic Effects:

Pregnancy Category X: Estrogens should not be used during pregnancy. See CONTRAINDICATIONS and Boxed WARNINGS.

Nursing Mothers:

As a general principle, the administration of any drug to nursing mothers should be done only when clearly necessary since many drugs are excreted in human milk. In addition, estrogen administration to nursing mothers has been shown to decrease the quantity and quality of the milk.

Adverse Reactions:

The following additional adverse reactions have been reported with estrogen therapy: (see WARNINGS regarding induction of neoplasia, adverse effects on the fetus, increased incidence of gallbladder disease, cardiovascular disease, elevated blood pressure, and hypercalcemia.)

Genitourinary System:

Changes in vaginal bleeding pattern and abnormal withdrawal bleeding or flow; breakthrough bleeding, spotting.

Increase in size of uterine leiomyomata.

Vaginal candidiasis.

Change in amount of cervical secretion.

Breasts:

Tenderness, enlargement.

Gastrointestinal:

Nausea, vomiting.

Abdominal cramps, bloating.

Cholestatic jaundice.

Increased incidence of gallbladder disease.

Skin:

Chloasma or melasma that may persist when drug is discontinued.

Erythema multiforme.

Erythema nodosum.

Hemorrhagic eruption.

Loss of scalp hair.

Hirsutism.

Eyes:

Steepening of corneal curvature.

Intolerance to contact lenses.

Central Nervous System:

Headache, migraine, dizziness.

Mental depression.

Chorea.

Miscellaneous:

Increase or decrease in weight.

Reduced carbohydrate tolerance.

Aggravation of porphyria.

Edema.

Changes in libido.

Overdosage:

Serious ill effects have not been reported following acute ingestion of large doses of estrogen-containing oral contraceptives by young children. Overdosage of estrogen may cause nausea and vomiting, and withdrawal bleeding may occur in females.

Dosage and Administration:

1. For treatment of moderate to severe vasomotor symptoms, vulval and vaginal atrophy associated with the menopause, the lowest dose and regimen that will control symptoms should be chosen and medication should be discontinued as promptly as possible.
   Attempts to discontinue or taper medication should be made at 3 to 6 month intervals.
   Usual dosage ranges:
   Vasomotor symptoms: Estropipate tablets 0.75 mg to 6 mg per day. The lowest dose that will control symptoms should be chosen. If the patient has not menstruated within the last two months or more, cyclic administration is started arbitrarily. If the patient is menstruating, cyclic administration is started on day 5 of bleeding.
   Vulval and vaginal atrophy: Estropipate tablets 0.75 mg to 6 mg daily, depending upon the tissue response of the individual patient. The lowest dose that will control symptoms should be chosen. Administer cyclically.
2. For treatment of female hypoestrogenism due to hypogonadism, castration, or primary ovarian failure.
   Usual dosage ranges:
   Female hypogonadism: A daily dose of 1.5 mg to 9 mg of estropipate tablets may be given for the first three weeks of a theoretical cycle, followed by a rest period of eight to ten days. The lowest dose that will control symptoms should be chosen. If bleeding does not occur by the end of this period, the same dosage schedule is repeated. The number of courses of estrogen therapy necessary to produce bleeding may vary depending on the responsiveness of the endometrium. If satisfactory withdrawal bleeding does not occur, an oral progestogen may be given in addition to estrogen during the third week of the cycle.
   Female castration or primary ovarian failure: A daily dose of 1.5 mg to 9 mg of estropipate tablets may be given for the first three weeks of a theoretical cycle, followed by a rest period of eight to ten days. Adjust dosage upward or downward according to severity of symptoms and response of the patient. For maintenance, adjust dosage to lowest level that will provide effective control.
   Treated patients with an intact uterus should be monitored closely for signs of endometrial cancer and appropriate diagnostic measures should be taken to rule out malignancy in the event of persistent or recurring abnormal vaginal bleeding.
3. For prevention of osteoporosis. A daily dose of 0.75 mg of estropipate tablets for 25 days of a 31-day cycle per month.

How Supplied:

Estropipate Tablets, USP are available as:

0.75 mg: (calculated as sodium estrone sulfate 0.625 mg)

Yellow, round, flat-faced, beveled-edge, scored tablet. Debossed with stylized Barr on one side and 555/727 on the scored side. Available in bottles of:

21 NDC 0555-0727-38

100 NDC 0555-0727-02

500 NDC 0555-0727-04

1000 NDC 0555-0727-05

1.5 mg: (calculated as sodium estrone sulfate 1.25 mg)

Peach, round, flat-faced, beveled-edge, scored tablet. Debossed with stylized Barr on one side and 555/728 on the scored side. Available in bottles of:

21 NDC 0555-0728-38

100 NDC 0555-0728-02

500 NDC 0555-0728-04

1000 NDC 0555-0728-05

3 mg:(calculated as sodium estrone sulfate 2.5 mg)

Blue, round, flat-faced, beveled-edge, scored tablet. Debossed with stylized Barr on one side and 555/729 on the scored side. Available in bottles of:

21 NDC 0555-0729-38

100 NDC 0555-0729-02

500 NDC 0555-0729-04

1000 NDC 0555-0729-05

Dispense with a child-resistant closure in a tight, light-resistant container.

Store at controlled room temperature 15°-30°C (59°-86°F) [See USP].

INFORMATION FOR PATIENTS

ESTROPIPATE TABLETS, USP

INTRODUCTION:

This leaflet describes when and how to use estrogens, and the risks and benefits of estrogen treatment.

Estrogens have important benefits but also some risks. You must decide, with your doctor, whether the risks to you of estrogen use are acceptable because of their benefits. If you use estrogens, check with your doctor to be sure you are using the lowest possible dose that works, and that you don't use them longer than necessary. How long you need to use estrogens will depend on the reason for use.

USES OF ESTROGEN:

(Not every estrogen drug is approved for every use listed in this section. If you want to know which of these possible uses are approved for the medicine prescribed for you, ask your doctor or pharmacist to show you the professional labeling. You can also look up the specific estrogen product in a book called the “Physicians’ Desk Reference”, which is available in many book stores and public libraries. Generic drugs carry virtually the same labeling information as their brand name versions.)

• To reduce moderate or severe menopausal symptoms. Estrogens are hormones made by the ovaries of normal women. Between the ages 45 and 55, the ovaries normally stop making estrogens. This leads to a drop in body estrogen levels which causes the "change of life" or menopause (the end of monthly menstrual periods). If both ovaries are removed during an operation before natural menopause takes place, the sudden drop in estrogen levels causes "surgical menopause".
  When the estrogen levels begin dropping, some women develop very uncomfortable symptoms, such as feelings of warmth in the face, neck, and chest, or sudden intense episodes of heat and sweating ("hot flashes" or "hot flushes"). Using estrogen drugs can help the body adjust to lower estrogen levels and reduce these symptoms. Most women have only mild menopausal symptoms or none at all and do not need to use estrogen drugs for these symptoms. Others may need to take estrogens for a few months while their bodies adjust to lower estrogen levels. The majority of women do not need estrogen replacement for longer than six months for these symptoms.
• To treat vulval and vaginal atrophy (itching, burning, dryness in or around the vagina, difficulty or burning on urination) associated with menopause.
• To treat certain conditions in which a young woman's ovaries do not produce enough estrogen naturally.
• To treat certain types of abnormal vaginal bleeding due to hormonal imbalance when your doctor has found no serious cause of the bleeding.
• To treat certain cancers in special situations, in men and women.
• To prevent thinning of bones.
  Osteoporosis is a thinning of the bones that makes them weaker and allows them to break more easily. The bones of the spine, wrists and hips break most often in osteoporosis. Both men and women start to lose bone mass after about age 40, but women lose bone mass faster after the menopause. Using estrogens after the menopause slows down bone thinning and may prevent bones from breaking. Lifelong adequate calcium intake, either in the diet (such as dairy products) or by calcium supplements (to reach a total daily intake of 1000 milligrams per day before menopause or 1500 milligrams per day after menopause), may help to prevent osteoporosis. Regular weight-bearing exercise (like walking and running for an hour, two or three times a week) may also help to prevent osteoporosis. Before you change your calcium intake or exercise habits, it is important to discuss these lifestyle changes with your doctor to find out if they are safe for you.
  Since estrogen use has some risks, only women who are likely to develop osteoporosis should use estrogens for prevention. Women who are likely to develop osteoporosis often have the following characteristics: white or Asian race, slim, cigarette smokers, and a family history of osteoporosis in a mother, sister, or aunt. Women who have relatively early menopause, often because their ovaries were removed during an operation (“surgical menopause”), are more likely to develop osteoporosis than women whose menopause happens at the average age.

WHO SHOULD NOT USE ESTROGENS:

Estrogens should not be used:

• During pregnancy (see boxed WARNINGS).
  If you think you may be pregnant, do not use any form of estrogen-containing drug. Using estrogens while you are pregnant may cause your unborn child to have birth defects. Estrogens do not prevent miscarriage.
• If you have unusual vaginal bleeding which has not been evaluated by your doctor (see boxed WARNINGS).
  Unusual vaginal bleeding can be a warning sign of cancer of the uterus, especially if it happens after menopause. Your doctor must find out the cause of the bleeding so that he or she can recommend the proper treatment. Taking estrogens without visiting your doctor can cause you serious harm if your vaginal bleeding is caused by cancer of the uterus.
• If you have had cancer.
  Since estrogens increase the risk of certain types of cancer, you should not use estrogens if you have ever had cancer of the breast or uterus, unless your doctor recommends that the drug may help in the cancer treatment. (For certain patients with breast or prostate cancer, estrogens may help.)
• If you have any circulation problems.
  Estrogen drugs should not be used except in unusually special situations in which your doctor judges that you need estrogen therapy so much that the risks are acceptable. Men and women with abnormal blood clotting conditions should avoid estrogen use (see DANGERS OF ESTROGENS, below).
• When they do not work.
  During menopause, some women develop nervous symptoms or depression. Estrogens do not relieve these symptoms. You may have heard that taking estrogens for years after menopause will keep your skin soft and supple and keep you feeling young. There is no evidence for these claims and such long-term estrogen use may have serious risks.
• After childbirth or when breastfeeding a baby:
  Estrogens should not be used to try to stop the breasts from filling with milk after a baby is born. Such treatment may increase the risk of developing blood clots (see DANGERS OF ESTROGENS, below).
  If you are breastfeeding, you should avoid using any drugs because many drugs pass through to the baby in the milk. While nursing a baby, you should take drugs only on the advice of your health care provider.

DANGERS OF ESTROGENS:

• Cancer of the uterus.
  Your risk of developing cancer of the uterus gets higher the longer you use estrogens and the larger doses you use. One study showed that after women stop taking estrogens, this higher cancer risk quickly returns to the usual level of risk (as if you had never used estrogen therapy). Three other studies showed that the cancer risk stayed high for 8 to more than 15 years after stopping estrogen treatment. Because of this risk, IT IS IMPORTANT TO TAKE THE LOWEST DOSE THAT WORKS AND TO TAKE IT ONLY AS LONG AS YOU NEED IT.
  Using progestin therapy together with estrogen therapy may reduce the higher risk of uterine cancer related to estrogen use (but see OTHER INFORMATION below).
  If you have had your uterus removed (total hysterectomy), there is no danger of developing cancer of the uterus.
• Cancer of the breast.
  Most studies have not shown a higher risk of breast cancer in women who have ever used estrogens. However, some studies have reported that breast cancer developed more often (up to twice the usual rate) in women who used estrogens for long periods of time (especially more than 10 years), or who used higher doses for shorter time periods.
  Regular breast examinations by a health professional and monthly self-examination are recommended for all women.
• Gallbladder disease.
  Women who use estrogens after menopause are more likely to develop gallbladder disease needing surgery than women who do not use estrogens.
• Abnormal blood clotting.
  Taking estrogens may cause changes in your blood clotting system. These changes allow the blood to clot more easily, possibly allowing clots to form in your bloodstream. If blood clots do form in your bloodstream, they can cut off the blood supply to vital organs, causing serious problems. These problems may include a stroke (by cutting off blood to the brain), a heart attack (by cutting off blood to the heart), a pulmonary embolus (by cutting off blood to the lungs), or other problems. Any of these conditions may cause death or serious long term disability. However, most studies of low dose estrogen usage by women do not show an increased risk of these complications.

SIDE EFFECTS:

In addition to the risks listed above, the following side effects have been reported with estrogen use:

Nausea and vomiting.

Breast tenderness or enlargement.

Enlargement of benign tumors ("fibroids") of the uterus.

Retention of excess fluid. This may make some conditions worsen, such as asthma, epilepsy, migraine, heart disease, or kidney disease.

A spotty darkening of the skin, particularly on the face.

REDUCING RISK OF ESTROGEN USE:

If you use estrogens, you can reduce your risks by doing these things:

• See your doctor regularly. While you are using estrogens, it is important to visit your doctor at least once a year for a check-up. If you develop vaginal bleeding while taking estrogens, you may need further evaluation. If members of your family have had breast cancer or if you have ever had breast lumps or an abnormal mammogram (breast x-ray), you may need to have more frequent breast examinations.
• Reassess your need for estrogens. You and your doctor should reevaluate whether or not you still need estrogens at least every six months.
• Be alert for signs of trouble. If any of these warning signals (or any other unusual symptoms) happen while you are using estrogens, call your doctor immediately:
  Abnormal bleeding from the vagina (possible uterine cancer)
  Pains in the calves or chest, sudden shortness of breath or coughing blood (possible clot in the legs, heart, or lungs)
  Severe headache or vomiting, dizziness, faintness, changes in vision or speech, weakness or numbness of an arm or leg (possible clot in the brain or eye)
  Breast lumps (possible breast cancer; ask your doctor or health professional to show you how to examine your breasts monthly)
  Yellowing of the skin or eyes (possible liver problem)
  Pain, swelling, or tenderness in the abdomen (possible gallbladder problem)

OTHER INFORMATION:

Estrogens increase the risk of developing a condition (endometrial hyperplasia) that may lead to cancer of the lining of the uterus. Taking progestins, another hormone drug, with estrogens lowers the risk of developing this condition. Therefore, if your uterus has not been removed, your doctor may prescribe a progestin for you to take together with the estrogen.

You should know, however, that taking estrogens with progestins may have additional risks. These include:

• unhealthy effects on blood fats (especially the lowering of HDL blood cholesterol, the “good” blood fat which protects against heart disease);
• unhealthy effects on blood sugar (which might make a diabetic condition worse); and
• a possible further increase in breast cancer risk which may be associated with long-term estrogen use.

Some research has shown that taking estrogens without progestins may protect women against developing heart disease. However, this is not certain. The protection shown may have been caused by the characteristics of the estrogen-treated women, and not by the estrogen treatment itself. In general, treated women were slimmer, more physically active, and were less likely to have diabetes than the untreated women. These characteristics are known to protect against heart disease.

You are cautioned to discuss very carefully with your doctor or health care provider all the possible risks and benefits of long-term estrogen and progestin treatment as they affect you personally.

Your doctor has prescribed this drug for you and you alone. Do not give the drug to anyone else.

If you will be taking calcium supplements as part of the treatment to help prevent osteoporosis, check with your doctor about how much to take.

Keep this and all drugs out of the reach of children. In case of overdose, call your doctor, hospital or poison control center immediately.

This leaflet provides a summary of the most important information about estrogens. If you want more information, ask your doctor or pharmacist to show you the professional labeling. The professional labeling is also published in a book called the "Physicians' Desk Reference," which is available in book stores and public libraries. Generic drugs carry virtually the same labeling information as their brand name versions.

HOW SUPPLIED:

Estropipate Tablets, USP are available as:

0.75 mg: (calculated as sodium estrone sulfate 0.625 mg)

Yellow, round, flat-faced, beveled-edge, scored tablet. Debossed with stylized Barr on one side and 555/727 on the scored side. Available in bottles of:

21 NDC 0555-0727-38

100 NDC 0555-0727-02

500 NDC 0555-0727-04

1000 NDC 0555-0727-05

1.5 mg: (calculated as sodium estrone sulfate 1.25 mg)

Peach, round, flat-faced, beveled-edge, sscored tablet. Debossed with stylized Barr on one side and 555/728 on the scored side. Available in bottles of:

21 NDC 0555-0728-38

100 NDC 0555-0728-02

500 NDC 0555-0728-04

1000 NDC 0555-0728-05

3 mg: (calculated as sodium estrone sulfate 2.5 mg)

Blue, round, flat-faced, beveled-edge, scored tablet. Debossed with stylized Barr on one side and 555/729 on the scored side. Available in bottles of:

21 NDC 0555-0729-38

100 NDC 0555-0729-02

500 NDC 0555-0729-04

1000 NDC 0555-0729-05

Store at controlled room temperature 15°-30°C (59°-86°F).

MANUFACTURED BY

BARR LABORATORIES, INC.

POMONA, NY 10970

PL-727,728,729Revised SEPTEMBER 2002

PRINCIPAL DISPLAY PANEL

Estropipate Tablets, USP 0.75 mg 100 Tablets Label Text

barr®

Laboratories, Inc.

NDC 0555-0727-02

Estropipate

Tablets, USP

0.75 mg

Rx only

100 Tablets

PRINCIPAL DISPLAY PANEL

Estropipate Tablets, USP 1.5 mg 100 Tablets Label Text

BARR LABORATORIES, INC.

NDC 0555-0728-02

Estropipate

Tablets, USP

1.5 mg

Rx only

100 Tablets

PRINCIPAL DISPLAY PANEL

Estropipate Tablets, USP 3 mg 100 Tablets Label Text

BARR LABORATORIES, INC.

NDC 0555-0729-02

Estropipate

Tablets, USP

3 mg

Rx only

100 Tablets

ESTROPIPATE  estropipate   tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0555-0727 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ESTROPIPATE (ESTROPIPATE) ESTROPIPATE 0.75 mg

Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE   CROSPOVIDONE   LACTOSE MONOHYDRATE   MAGNESIUM STEARATE   STARCH, CORN   D&C YELLOW NO. 10   FD&C YELLOW NO. 6   ALUMINUM OXIDE

Product Characteristics Color YELLOW Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code Barr;555;727 Contains

Packaging # NDC Package Description Multilevel Packaging 1 0555-0727-38 21 TABLET In 1 BOTTLE None 2 0555-0727-02 100 TABLET In 1 BOTTLE None 3 0555-0727-04 500 TABLET In 1 BOTTLE None 4 0555-0727-05 1000 TABLET In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA040135	01/18/2011

ESTROPIPATE  estropipate   tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0555-0728 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ESTROPIPATE (ESTROPIPATE) ESTROPIPATE 1.5 mg

Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE   CROSPOVIDONE   LACTOSE MONOHYDRATE   MAGNESIUM STEARATE   STARCH, CORN   FD&C YELLOW NO. 6   ALUMINUM OXIDE

Product Characteristics Color ORANGE (Peach) Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code Barr;555;728 Contains

Packaging # NDC Package Description Multilevel Packaging 1 0555-0728-38 21 TABLET In 1 BOTTLE None 2 0555-0728-02 100 TABLET In 1 BOTTLE None 3 0555-0728-04 500 TABLET In 1 BOTTLE None 4 0555-0728-05 1000 TABLET In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA040135	01/18/2011

ESTROPIPATE  estropipate   tablet

Product Information Product Type HUMAN PRESCRIPTION DRUG NDC Product Code (Source) 0555-0729 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ESTROPIPATE (ESTROPIPATE) ESTROPIPATE 3 mg

Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE   CROSPOVIDONE   LACTOSE MONOHYDRATE   MAGNESIUM STEARATE   STARCH, CORN   FD&C BLUE NO. 2   ALUMINUM OXIDE

Product Characteristics Color BLUE Score 2 pieces Shape ROUND Size 9mm Flavor Imprint Code Barr;555;729 Contains

Packaging # NDC Package Description Multilevel Packaging 1 0555-0729-38 21 TABLET In 1 BOTTLE None 2 0555-0729-02 100 TABLET In 1 BOTTLE None 3 0555-0729-04 500 TABLET In 1 BOTTLE None 4 0555-0729-05 1000 TABLET In 1 BOTTLE None

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA040135	01/18/2011

Labeler - Barr Laboratories Inc. (802716563)

Revised: 01/2011Barr Laboratories Inc.