zidovudine - 53104-0105-4 - (zidovudine)

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Drug Information of zidovudine

Product NDC: 53104-0105
Proprietary Name: zidovudine
Non Proprietary Name: zidovudine
Active Ingredient(s): 50    mg/5mL & nbsp;   zidovudine
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of zidovudine

Product NDC: 53104-0105
Labeler Name: Cipla Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077981
Marketing Category: ANDA
Start Marketing Date: 20080626

Package Information of zidovudine

Package NDC: 53104-0105-4
Package Description: 100 mL in 1 BOTTLE (53104-0105-4)

NDC Information of zidovudine

NDC Code 53104-0105-4
Proprietary Name zidovudine
Package Description 100 mL in 1 BOTTLE (53104-0105-4)
Product NDC 53104-0105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name zidovudine
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20080626
Marketing Category Name ANDA
Labeler Name Cipla Limited
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