Zidovudine - 52343-045-60 - (Zidovudine)

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Drug Information of Zidovudine

Product NDC: 52343-045
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: 52343-045
Labeler Name: Gen-Source Rx
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077267
Marketing Category: ANDA
Start Marketing Date: 20050919

Package Information of Zidovudine

Package NDC: 52343-045-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (52343-045-60)

NDC Information of Zidovudine

NDC Code 52343-045-60
Proprietary Name Zidovudine
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (52343-045-60)
Product NDC 52343-045
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zidovudine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050919
Marketing Category Name ANDA
Labeler Name Gen-Source Rx
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