"60505-1308-2" National Drug Code (NDC)

Ciprofloxacin 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60505-1308-2)
(Apotex Corp)

NDC Code60505-1308-2
Package Description20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60505-1308-2)
Product NDC60505-1308
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20050419
Marketing Category NameANDA
Application NumberANDA076896
ManufacturerApotex Corp
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

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