"49349-867-02" National Drug Code (NDC)

Zidovudine 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-867-02)
(REMEDYREPACK INC.)

NDC Code49349-867-02
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (49349-867-02)
Product NDC49349-867
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZidovudine
Non-Proprietary NameZidovudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130415
Marketing Category NameANDA
Application NumberANDA077267
ManufacturerREMEDYREPACK INC.
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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