NDC 42794-006 Ergocalciferol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42794 - Sigmapharm Laboratories, Llc
- 42794-006 - Ergocalciferol
Product Characteristics
Product Packages
NDC Code 42794-006-02
Package Description: 100 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Details
What is NDC 42794-006?
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:
- SOYBEAN OIL (UNII: 241ATL177A)
- GELATIN (UNII: 2G86QN327L)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
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
* Please review the disclaimer below.
[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".