NDC 54868-5416 Epivir
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5416 - Epivir
Product Characteristics
GRAY (C48324)
17 MM
GX;EJ7
1
Product Packages
NDC Code 54868-5416-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5416?
What are the uses for Epivir?
Which are Epivir UNII Codes?
The UNII codes for the active ingredients in this product are:
- LAMIVUDINE (UNII: 2T8Q726O95)
- LAMIVUDINE (UNII: 2T8Q726O95) (Active Moiety)
Which are Epivir 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:
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE BLACK (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Epivir?
- RxCUI: 152931 - Epivir 150 MG Oral Tablet
- RxCUI: 152931 - lamivudine 150 MG Oral Tablet [Epivir]
- RxCUI: 152931 - 3TC 150 MG Oral Tablet [Epivir]
- RxCUI: 199147 - lamiVUDine 150 MG Oral Tablet
- RxCUI: 199147 - lamivudine 150 MG Oral Tablet
* 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".