Zidovudine - 48792-7809-6 - (Zidovudine)

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Drug Information of Zidovudine

Product NDC: 48792-7809
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: 48792-7809
Labeler Name: Sunshine Lake Pharma Co., Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202058
Marketing Category: ANDA
Start Marketing Date: 20120901

Package Information of Zidovudine

Package NDC: 48792-7809-6
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7809-6)

NDC Information of Zidovudine

NDC Code 48792-7809-6
Proprietary Name Zidovudine
Package Description 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7809-6)
Product NDC 48792-7809
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zidovudine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120901
Marketing Category Name ANDA
Labeler Name Sunshine Lake Pharma Co., Ltd.
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