NDC 10544-527 Ergocalciferol
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Product Details
What is NDC 10544-527?
What are the uses for Ergocalciferol?
Which are Ergocalciferol UNII Codes?
The UNII codes for the active ingredients in this product are:
- ERGOCALCIFEROL (UNII: VS041H42XC)
- ERGOCALCIFEROL (UNII: VS041H42XC) (Active Moiety)
Which are Ergocalciferol Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SOYBEAN OIL (UNII: 241ATL177A)
What is the NDC to RxNorm Crosswalk for Ergocalciferol?
- RxCUI: 1367410 - ergocalciferol 1.25 MG (50,000 UNT) Oral Capsule
- RxCUI: 1367410 - ergocalciferol 1.25 MG Oral Capsule
- RxCUI: 1367410 - vitamin D 1.25 MG Oral Capsule
- RxCUI: 1367410 - vitamin D2 1250 MCG Oral Capsule
- RxCUI: 1367410 - vitamin D2 50,000 UNT Oral Capsule
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Patient Education
Ergocalciferol
Ergocalciferol is used in the treatment of hypoparathyroidism (condition in which the body does not produce enough parathyroid hormone), refractory rickets (softening and weakening of bones that does not respond to treatment), and familial hypophosphatemia (rickets or osteomalacia caused by an inherited condition with a decreased ability to break down vitamin D in the body). Ergocalciferol is in a class of medications called vitamin D analogs. It works by helping the body to use more of the calcium found in foods or supplements.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".