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"48792-7809-6" National Drug Code (NDC)

Zidovudine 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7809-6)
(Sunshine Lake Pharma Co., Ltd.)

NDC Code48792-7809-6
Package Description60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7809-6)
Product NDC48792-7809
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZidovudine
Non-Proprietary NameZidovudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120901
Marketing Category NameANDA
Application NumberANDA202058
ManufacturerSunshine Lake Pharma Co., Ltd.
Substance NameZIDOVUDINE
Strength300
Strength Unitmg/1
Pharmacy ClassesHuman Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient],Nucleoside Reverse Transcriptase Inhibitors [MoA]

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