NDC 16590-061 Combivir
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa
- 16590-061 - Combivir
Product Characteristics
Product Packages
NDC Code 16590-061-10
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE
NDC Code 16590-061-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 16590-061?
What are the uses for Combivir?
Which are Combivir 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)
What is the NDC to RxNorm Crosswalk for Combivir?
- 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
- RxCUI: 213088 - COMBIVIR 150 MG / 300 MG Oral Tablet
- RxCUI: 213088 - lamivudine 150 MG / zidovudine 300 MG Oral Tablet [Combivir]
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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".