"16571-413-50" National Drug Code (NDC)

Ciprofloxacin 500 TABLET in 1 BOTTLE (16571-413-50)
(Rising Pharmaceuticals, Inc.)

NDC Code16571-413-50
Package Description500 TABLET in 1 BOTTLE (16571-413-50)
Product NDC16571-413
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20040910
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerRising Pharmaceuticals, Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength750
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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