Epivir - 49349-713-12 - (Lamivudine)

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Drug Information of Epivir

Product NDC: 49349-713
Proprietary Name: Epivir
Non Proprietary Name: Lamivudine
Active Ingredient(s): 300    mg/1 & nbsp;   Lamivudine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Epivir

Product NDC: 49349-713
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020564
Marketing Category: NDA
Start Marketing Date: 20110830

Package Information of Epivir

Package NDC: 49349-713-12
Package Description: 8 TABLET in 1 BLISTER PACK (49349-713-12)

NDC Information of Epivir

NDC Code 49349-713-12
Proprietary Name Epivir
Package Description 8 TABLET in 1 BLISTER PACK (49349-713-12)
Product NDC 49349-713
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamivudine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110830
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name LAMIVUDINE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Epivir


General Information