Zidovudine - 64376-129-23 - (Zidovudine)

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Drug Information of Zidovudine

Product NDC: 64376-129
Proprietary Name: Zidovudine
Non Proprietary Name: Zidovudine
Active Ingredient(s): 50    mg/5mL & nbsp;   Zidovudine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Zidovudine

Product NDC: 64376-129
Labeler Name: Boca Pharmacal Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077981
Marketing Category: ANDA
Start Marketing Date: 20120817

Package Information of Zidovudine

Package NDC: 64376-129-23
Package Description: 240 mL in 1 BOTTLE (64376-129-23)

NDC Information of Zidovudine

NDC Code 64376-129-23
Proprietary Name Zidovudine
Package Description 240 mL in 1 BOTTLE (64376-129-23)
Product NDC 64376-129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zidovudine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20120817
Marketing Category Name ANDA
Labeler Name Boca Pharmacal Inc.
Substance Name ZIDOVUDINE
Strength Number 50
Strength Unit mg/5mL
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