NDC 54741-102 Lamivudine And Zidovudine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54741 - Shanghai Desano Bio-pharmaceutical Co., Ltd.
- 54741-102 - Lamivudine And Zidovudine
Product Characteristics
Product Packages
NDC Code 54741-102-01
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54741-102?
What are the uses for Lamivudine And Zidovudine?
Which are Lamivudine And Zidovudine UNII Codes?
The UNII codes for the active ingredients in this product are:
- LAMIVUDINE (UNII: 2T8Q726O95)
- LAMIVUDINE (UNII: 2T8Q726O95) (Active Moiety)
- ZIDOVUDINE (UNII: 4B9XT59T7S)
- ZIDOVUDINE (UNII: 4B9XT59T7S) (Active Moiety)
Which are Lamivudine And Zidovudine 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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Lamivudine And Zidovudine?
- RxCUI: 200082 - lamiVUDine 150 MG / zidovudine 300 MG Oral Tablet
- RxCUI: 200082 - lamivudine 150 MG / zidovudine 300 MG Oral Tablet
- RxCUI: 200082 - 3TC 150 MG / AZT 300 MG Oral Tablet
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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".