"68071-4260-2" National Drug Code (NDC)

Ciprofloxacin 21 TABLET in 1 BOTTLE (68071-4260-2)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-4260-2
Package Description21 TABLET in 1 BOTTLE (68071-4260-2)
Product NDC68071-4260
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20040910
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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