"66267-919-21" National Drug Code (NDC)

Ciprofloxacin 21 TABLET in 1 BOTTLE (66267-919-21)
(NuCare Pharmaceuticals, Inc.)

NDC Code66267-919-21
Package Description21 TABLET in 1 BOTTLE (66267-919-21)
Product NDC66267-919
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
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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