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"53808-0812-1" National Drug Code (NDC)

Zidovudine 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0812-1)
(DOH CENTRAL PHARMACY)

NDC Code53808-0812-1
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (53808-0812-1)
Product NDC53808-0812
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameZidovudine
Non-Proprietary NameZidovudine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20090701
Marketing Category NameANDA
Application NumberANDA077267
ManufacturerDOH CENTRAL PHARMACY
Substance NameZIDOVUDINE
Strength300
Strength Unitmg/1
Pharmacy ClassesHuman Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleoside Analog [EXT],Nucleoside Reverse Transcriptase Inhibitors [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/53808-0812-1





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