Ergocalciferol (ergocalciferol) - Dosing, PA Forms & Info (2026)
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    1. Home
    2. Ergocalciferol - Ergocalciferol capsule

    Get your patient on Ergocalciferol - Ergocalciferol capsule (Ergocalciferol)

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    Ergocalciferol - Ergocalciferol capsule prescribing information

    • Indications & usage
    • Dosage & administration
    • Contraindications
    • Adverse reactions
    • Drug interactions
    • Description
    • Pharmacology
    • How supplied/storage & handling
    • Data source
    • Indications & usage
    • Dosage & administration
    • Contraindications
    • Adverse reactions
    • Drug interactions
    • Description
    • Pharmacology
    • How supplied/storage & handling
    • Data source
    Prescribing Information
    Indications & Usage

    INDICATIONS  AND  USAGE

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

    Dosage & Administration

    DOSAGE AND  ADMINISTRATION

    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.

    Contraindications

    CONTRAINDICATIONS

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

    Adverse Reactions

    ADVERSE REACTIONS

    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.

    Drug Interactions

    Drug Interactions

    Mineral oil interferes with the absorption of fat-soluble vitamins, including vitamin D preparations. Administration of thiazide diuretics to hypoparathyroid patients who are concurrently being treated with ergocalciferol may cause hypercalcemia.

    Description

    DESCRIPTION

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

    Each softgel capsule, for oral administration, contains Ergocalciferol, USP 1.25 mg (equivalent to 50,000 USP units of Vitamin D), in an edible vegetable oil.

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

    Inactive Ingredients : D&C Yellow No. 10, FD&C Blue No. 1, Gelatin, Glycerin, Purified Water, Refined Soybean Oil.

    Pharmacology

    CLINICAL PHARMACOLOGY

    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-dihydroxy- vitamin 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.

    How Supplied/Storage & Handling

    HOW SUPPLIED

    Each green, oval softgel capsule is imprinted with A3 and contains 1.25 mg (50,000 USP units vitamin D) of ergocalciferol, USP.

    NDC 62332-464-31 Bottles of 100 Softgel Capsules
    Store at 20°- 25°C (68°-77°F) [See USP Controlled Room Temperature].

    Protect from light and moisture.

    Dispense in a tight, light-resistant container as defined in the USP.


    To report SUSPECTED ADVERSE REACTIONS, contact Alembic Pharmaceuticals Limited at 1-866-210-9797 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch

    Manufactured by:

    Swiss Caps AG

    Kirchberg, Switzerland

    Manufactured for:

    Alembic Pharmaceuticals, Inc.

    Bedminster, NJ 07921, USA


    Revision: 08/2021

    Data SourceWe receive information directly from the FDA and PrescriberPoint is updated as frequently as changes are made available
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