"68071-2391-2" National Drug Code (NDC)

Ciprofloxacin 20 TABLET, FILM COATED in 1 BOTTLE (68071-2391-2)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-2391-2
Package Description20 TABLET, FILM COATED in 1 BOTTLE (68071-2391-2)
Product NDC68071-2391
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20040609
Marketing Category NameANDA
Application NumberANDA075593
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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