Zidovudine - 53104-0100-6 - (zidovudine)

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Drug Information of Zidovudine

Product NDC: 53104-0100
Proprietary Name: Zidovudine
Non Proprietary Name: zidovudine
Active Ingredient(s): 100    mg/1 & nbsp;   zidovudine
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Zidovudine

Product NDC: 53104-0100
Labeler Name: Cipla Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078349
Marketing Category: ANDA
Start Marketing Date: 20070523

Package Information of Zidovudine

Package NDC: 53104-0100-6
Package Description: 1000 CAPSULE in 1 BOTTLE (53104-0100-6)

NDC Information of Zidovudine

NDC Code 53104-0100-6
Proprietary Name Zidovudine
Package Description 1000 CAPSULE in 1 BOTTLE (53104-0100-6)
Product NDC 53104-0100
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zidovudine
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070523
Marketing Category Name ANDA
Labeler Name Cipla Limited
Substance Name ZIDOVUDINE
Strength Number 100
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