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Lamivudine and Zidovudine - 49349-896-12 - (Lamivudine and Zidovudine)

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Drug Information of Lamivudine and Zidovudine

Product NDC: 49349-896
Proprietary Name: Lamivudine and Zidovudine
Non Proprietary Name: Lamivudine and Zidovudine
Active Ingredient(s): 150    mg/1 & nbsp;   Lamivudine and Zidovudine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lamivudine and Zidovudine

Product NDC: 49349-896
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079081
Marketing Category: ANDA
Start Marketing Date: 20130411

Package Information of Lamivudine and Zidovudine

Package NDC: 49349-896-12
Package Description: 8 TABLET, FILM COATED in 1 BLISTER PACK (49349-896-12)

NDC Information of Lamivudine and Zidovudine

NDC Code 49349-896-12
Proprietary Name Lamivudine and Zidovudine
Package Description 8 TABLET, FILM COATED in 1 BLISTER PACK (49349-896-12)
Product NDC 49349-896
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lamivudine and Zidovudine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130411
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LAMIVUDINE
Strength Number 150
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 Lamivudine and Zidovudine


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