NOVAREL- gonadotrophin, chorionic
Ferring Pharmaceuticals Inc.
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Human chorionic gonadotropin (HCG), a polypeptide hormone produced by the human placenta, is composed of an alpha and a beta subunit. The alpha subunit is essentially identical to the alpha subunits of the human pituitary gonadotropins, luteinizing hormone (LH) and follicle-stimulating hormone (FSH), as well as to the alpha subunit of human thyroid-stimulating hormone (TSH). The beta subunits of these hormones differ in amino acid sequence.
NOVAREL (chorionic gonadotropin) for injection is a water soluble glycoprotein derived from human pregnancy urine and administered intramuscularly after reconstitution. The sterile lyophilized powder is stable. When reconstituted with Bacteriostatic Water for Injection preserved with benzyl alcohol 0.9%, the solution should be refrigerated and used within 30 days.
Each 5,000 USP units vial contains:
chorionic gonadotropin 5,000 USP Units, Dibasic Sodium Phosphate 16 mg, Mannitol 100 mg, and Monobasic Sodium Phosphate 4 mg.
Each 10,000 USP units vial contains:
chorionic gonadotropin 10,000 USP Units, Dibasic Sodium Phosphate 16 mg, Mannitol 100 mg, and Monobasic Sodium Phosphate 4 mg.
The action of HCG is virtually identical to that of pituitary LH, although HCG appears to have a small degree of FSH activity as well. It stimulates production of gonadal steroid hormones by stimulating the interstitial cells (Leydig cells) of the testis to produce androgens and the corpus luteum of the ovary to produce progesterone. Androgen stimulation in the male leads to the development of secondary sex characteristics and may stimulate testicular descent when no anatomical impediment to descent is present. This descent is usually reversible when HCG is discontinued. During the normal menstrual cycle, LH participates with FSH in the development and maturation of the normal ovarian follicle, and the mid-cycle LH surge triggers ovulation. HCG can substitute for LH in this function.
During a normal pregnancy, HCG secreted by the placenta maintains the corpus luteum after LH secretion decreases, supporting continued secretion of estrogen and progesterone, and preventing menstruation. HCG HAS NO KNOWN EFFECT ON FAT MOBILIZATION, APPETITE OR SENSE OF HUNGER, OR BODY FAT DISTRIBUTION.
HCG HAS NOT BEEN DEMONSTRATED TO BE EFFECTIVE ADJUNCTIVE THERAPY IN THE TREATMENT OF OBESITY. THERE IS NO SUBSTANTIAL EVIDENCE THAT IT INCREASES WEIGHT LOSS BEYOND THAT RESULTING FROM CALORIC RESTRICTION, THAT IT CAUSES A MORE ATTRACTIVE OR "NORMAL" DISTRIBUTION OF FAT, OR THAT IT DECREASES THE HUNGER AND DISCOMFORT ASSOCIATED WITH CALORIE-RESTRICTED DIETS.
Precocious puberty, prostatic carcinoma or other androgen-dependent neoplasm, prior allergic reaction to HCG. HCG may cause fetal harm when administered to a pregnant woman. Combined HCG/PMS (pregnant mare's serum) therapy has been noted to induce high incidences of external congenital anomalies in the offspring of mice, in a dose-dependent manner. The potential extrapolation to humans has not been determined.
HCG should be used in conjunction with human menopausal gonadotropins only by physicians experienced with infertility problems who are familiar with the criteria for patient selection, contraindications, warnings, precautions, and adverse reactions described in the package insert for menotropins. The principal serious adverse reactions during this use are: (1) Ovarian hyperstimulation, a syndrome of sudden ovarian enlargement, ascites with or without pain, and/or pleural effusion; (2) Enlargement of preexisting ovarian cysts or rupture of ovarian cysts with resultant hemoperitoneum; (3) Multiple births, and (4) Arterial thromboembolism.
The recommended diluent for reconstitution is Bacteriostatic Water for Injection preserved with benzyl alcohol 0.9%. Benzyl alcohol has been reported to be associated with a fatal "Gasping Syndrome" in premature infants.
Anaphylaxis has been reported with urinary-derived HCG products.
HCG can crossreact in the radioimmunoassay of gonadotropins, especially luteinizing hormone. Each individual laboratory should establish the degree of crossreactivity with their gonadotropin assay. Physicians should make the laboratory aware of patients on HCG if gonadotropin levels are requested.
There have been sporadic reports of testicular tumors in otherwise healthy young men receiving HCG for secondary infertility. A causative relationship between HCG and tumor development in these men has not been established. Defects of forelimbs and of the central nervous system, as well as alterations in sex ratio, have been reported in mice on combined gonadotropin and HCG regimens. The dose of gonadotropin used was intended to induce superovulation. No mutagenic effect has been clearly established in humans. Fertility—see "INDICATIONS AND USAGE."
See "CONTRAINDICATIONS" section. Combined HCG/PMS (pregnant mare's serum) therapy has been noted to induce high incidences of external congenital anomalies in the offspring of mice, in a dose-dependent manner. The potential extrapolation to humans has not been determined.
(see WARNINGS) Headache, irritability, restlessness, depression, fatigue, edema, precocious puberty, gynecomastia, pain at the site of injection. Hypersensitivity reactions both localized and systemic in nature, including erythema, urticaria, rash, angioedema, dyspnea and shortness of breath, have been reported. The relationship of these allergic-like events to the polypeptide hormone or the diluent containing benzyl alcohol is not clear.
(Intramuscular Use Only): The dosage regimen employed in any particular case will depend upon the indication for use, the age and weight of the patient, and the physician's preference. The following regimens have been advocated by various authorities.
Prepubertal cryptorchidism not due to anatomical obstruction:
Selected cases of hypogonadotropic hypogonadism in males:
Reconstitution volume of bacteriostatic water for injection | 10,000 IU Vial Concentration | 5,000 IU Vial Concentration | Administration |
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1 mL | 10,000 IU/mL | 5,000 IU/mL | Administer entire dose at once |
10 mL | 1,000 IU/mL | 500 IU/mL | Multiple dose administration, refrigerate between doses |
NOTE: Prior to diluting NOVAREL with Bacteriostatic Water for Injection (Table 1):
Induction of ovulation and pregnancy in the anovulatory, infertile woman in whom the cause of anovulation is secondary and not due to primary ovarian failure and who has been appropriately pretreated with human menotropins (See prescribing information for menotropins for dosage and administration for that drug product).
5,000 to 10,000 USP Units one day following the last dose of menotropins. (A dosage of 10,000 USP Units is recommended in the labeling for menotropins).
Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
To safely dispose of medical sharps, place used needles and syringes in a closeable, puncture-resistant container, such as a red biohazard sharps container. Sharps containers should then be taken to a collection center for proper disposal. Ask your physician or pharmacist or reference our website for more information about safely disposing used sharps.
In some states, it is illegal to throw away medical sharps in household garbage, recycling, and compost bins. Needles and other sharps must be placed in an approved sharps container and disposed of at an approved drop-off site.
NOVAREL (chorionic gonadotropin) for Injection, USP, is available as individually packaged multiple-dose vials containing 5,000 or 10,000 USP Units per vial.
Each vial of NOVAREL is accompanied by a vial of sterile diluent containing 10 mL of Bacteriostatic Water for Injection, USP containing 0.9% benzyl alcohol.
NOVAREL is available in the following presentations:
Manufactured by:
Ferring Pharmaceuticals Inc.
Parsippany, NJ 07054
U.S. License No. 2112
XXXXXXXXXX
Rev. 05/2023
NDC 55566-1501-1
Rx only
chorionic gonadotropin
Novarel®
for injection
10,000 USP units
for intramuscular use only
1 multiple-dose vial of Chorionic Gonadotropin
for Injection
1 multiple-dose vial of
Bacteriostatic Water
for injection, USP, 10 mL
FERRING
PHARMACEUTICALS
NDC 55566-1502-1
Rx only
chorionic gonadotropin
Novarel®
for injection
5,000 USP units
for intramuscular use only
1 multiple-dose vial of Chorionic Gonadotropin
for Injection
1 multiple-dose vial of
Bacteriostatic Water
for injection, USP, 10 mL
FERRING
PHARMACEUTICALS
NOVAREL
gonadotrophin, chorionic kit |
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NOVAREL
gonadotrophin, chorionic kit |
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Labeler - Ferring Pharmaceuticals Inc. (103722955) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
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Ferring Production Inc. | 079510999 | manufacture(55566-1502) , pack(55566-1502, 55566-1501) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Jubilant HollisterStier General Partnership | 246762764 | manufacture(55566-1501, 55566-1502) , pack(55566-1501, 55566-1502) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Ferring GmbH | 328609615 | manufacture(55566-1501) , pack(55566-1501) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Ferring International Center SA | 481210362 | pack(55566-1501) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Aspen Oss B.V. | 491017488 | api manufacture(55566-1501, 55566-1502) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Aspen Oss B.V. | 491013870 | api manufacture(55566-1501, 55566-1502) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
F.M. Howell & Company | 962888116 | pack(55566-1501) |
Establishment | |||
Name | Address | ID/FEI | Business Operations |
---|---|---|---|
Instituto Massone S.A. | 970053831 | api manufacture(55566-1501, 55566-1502) |