Zidovudine - 49349-867-12 - (Zidovudine)

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Drug Information of Zidovudine

Product NDC: 49349-867
Proprietary Name: Zidovudine
Non Proprietary Name: Zidovudine
Active Ingredient(s): 300    mg/1 & nbsp;   Zidovudine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Zidovudine

Product NDC: 49349-867
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077267
Marketing Category: ANDA
Start Marketing Date: 20130415

Package Information of Zidovudine

Package NDC: 49349-867-12
Package Description: 8 TABLET, FILM COATED in 1 BLISTER PACK (49349-867-12)

NDC Information of Zidovudine

NDC Code 49349-867-12
Proprietary Name Zidovudine
Package Description 8 TABLET, FILM COATED in 1 BLISTER PACK (49349-867-12)
Product NDC 49349-867
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zidovudine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130415
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name ZIDOVUDINE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Complete Information of Zidovudine


General Information