Label: VITAMIN D- ergocalciferol capsule

Ergocalciferol Capsules, USP are a synthetic calcium regulator for oral administration.

Ergocalciferol is a white, colorless crystal, insoluble in water, soluble in organic solvents, and slightly soluble in vegetable oils. It is affected by air and by light. Ergosterol or provitamin D 2is found in plants and yeast and has no antirachitic activity.

There are more than 10 substances belonging to a group of steroid compounds, classified as having vitamin D or antirachitic activity.

One USP unit of vitamin D 2is equivalent to one International Unit (IU), and 1 mcg of vitamin D 2is equal to 40 USP Units.

Each capsule contains Vitamin D (Ergocalciferol) 1.25 mg equivalent to 50,000 USP Units in an edible vegetable oil.

Ergocalciferol, also called vitamin D 2, is 9,10-secoergosta-5,7,10(19), 22-tetraen-3-ol, (3β,5Z,7E,22 E)-; (C 28H 44O) with a molecular weight of 396.65, and has the following structural formula:

Inactive Ingredients: FD&C Blue #1, FD&C Yellow #5, Gelatin, Glycerin, Lecithin, Medium chain triglyceride, Purified water, Shellac glaze, N-Butyl alcohol, Simethicone, Soybean oil and Titanium dioxide.

The in vivo synthesis of the major biologically active metabolites of vitamin D occurs in two steps. The first hydroxylation of ergocalciferol takes place in the liver (to 25-hydroxyvitamin D) and the second in the kidneys (to 1, 25-dihydroxyvitamin D). Vitamin D metabolites promote the active absorption of calcium and phosphorus by the small intestine, thus elevating serum calcium and phosphate levels sufficiently to permit bone mineralization. Vitamin D metabolites also mobilize calcium and phosphate from bone and probably increase the reabsorption of calcium and perhaps also of phosphate by the renal tubules.

There is a time lag of 10 to 24 hours between the administration of vitamin D and the initiation of its action in the body due to the necessity of synthesis of the active metabolites in the liver and kidneys. Parathyroid hormone is responsible for the regulation of this metabolism in the kidneys.

Ergocalciferol Capsules, USP are indicated for use in the treatment of hypoparathyroidism, refractory rickets, also known as vitamin D resistant rickets, and familial hypophosphatemia.

Ergocalciferol Capsules, USP are contraindicated in patients with hypercalcemia, malabsorption syndrome, abnormal sensitivity to the toxic effects of vitamin D, and hypervitaminosis D.

Hypersensitivity to vitamin D may be one etiologic factor in infants with idiopathic hypercalcemia. In these cases vitamin D must be strictly restricted.

Keep out of the reach of children.

Hypervitaminosis D is characterized by effects on the following organ system:

Renal:Impairment of renal function with polyuria, nocturia, polydipsia, hypercalciuria, reversible azotemia, hypertension, nephrocalcinosis, generalized vascular calcification, or irreversible renal insufficiency which may result in death.

CNS:Mental retardation.

Soft Tissues:Widespread calcification of the soft tissues, including the heart, blood vessels, renal tubules, and lungs.

Skeletal:Bone demineralization (osteoporosis) in adults occurs concomitantly.

Decline in the average rate of linear growth and increased mineralization of bones in infants and children (dwarfism) vague aches, stiffness, and weakness.

Gastrointestinal:Nausea, anorexia, constipation.

Metabolic:Mild acidosis, anemia, weight loss.

Call your doctor for medical advice about side effects. You may report side effects to Strides Pharma Inc. at 1-877-244-9825 or go to www.strides.com

THE RANGE BETWEEN THERAPEUTIC AND TOXIC DOSES IS NARROW.

Vitamin D Resistant Rickets:12,000 to 500,000 USP Units daily.

Hypoparathyroidism:50,000 to 200,000 USP Units daily concomitantly with calcium lactate 4 g, six times per day.

DOSAGE MUST BE INDIVIDUALIZED UNDER CLOSE MEDICAL SUPERVISION.

Calcium intake should be adequate. Blood calcium and phosphorus determinations must be made every 2 weeks or more frequently if necessary.

X-rays of the bones should be taken every month until condition is corrected and stabilized.

Each capsule contains Vitamin D (Ergocalciferol) 1.25 mg equivalent to 50,000 USP Units. The green colored oval shaped transparent soft gelatin capsules are imprinted with '194' in white and contain clear light yellow oily liquid.

NDC: 70518-1878-00

NDC: 70518-1878-01

NDC: 70518-1878-02

NDC: 70518-1878-03

NDC: 70518-1878-04

PACKAGING: 4 in 1 BOTTLE PLASTIC

PACKAGING: 12 in 1 BOTTLE PLASTIC

PACKAGING: 12 in 1 BLISTER PACK

PACKAGING: 4 in 1 BLISTER PACK

PACKAGING: 30 in 1 BOTTLE PLASTIC

Store at 20 to 25°C (68 to 77°F) [see USP Controlled Room Temperature].

Protect from light.

Repackaged and Distributed By:

Remedy Repack, Inc.

625 Kolter Dr. Suite #4 Indiana, PA 1-724-465-8762

DRUG: VITAMIN D

GENERIC: ergocalciferol

DOSAGE: CAPSULE

ADMINSTRATION: ORAL

NDC: 70518-1878-0

NDC: 70518-1878-1

NDC: 70518-1878-2

NDC: 70518-1878-3

NDC: 70518-1878-4

COLOR: green

SHAPE: CAPSULE

SCORE: No score

SIZE: 12 mm

IMPRINT: 194

PACKAGING: 4 in 1 BOTTLE PLASTIC

PACKAGING: 12 in 1 BOTTLE PLASTIC

PACKAGING: 12 in 1 BLISTER PACK

PACKAGING: 4 in 1 BLISTER PACK

PACKAGING: 30 in 1 BOTTLE PLASTIC

ACTIVE INGREDIENT(S):

• ERGOCALCIFEROL 1.25mg in 1

INACTIVE INGREDIENT(S):

• FD&C YELLOW NO. 5
• GELATIN
• GLYCERIN
• LECITHIN, SOYBEAN
• MEDIUM-CHAIN TRIGLYCERIDES
• WATER
• FD&C BLUE NO. 1
• SOYBEAN OIL
• TITANIUM DIOXIDE
• SHELLAC
• ETHYLENE GLYCOL MONOETHYL ETHER