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"61786-305-12" National Drug Code (NDC)

Zidovudine 8 TABLET, FILM COATED in 1 BLISTER PACK (61786-305-12)
(REMEDYREPACK INC.)

NDC Code61786-305-12
Package Description8 TABLET, FILM COATED in 1 BLISTER PACK (61786-305-12)
Product NDC61786-305
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZidovudine
Non-Proprietary NameZidovudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20150519
Marketing Category NameANDA
Application NumberANDA202058
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61786-305-12





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