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"16571-412-50" National Drug Code (NDC)

Ciprofloxacin 500 TABLET in 1 BOTTLE (16571-412-50)
(Rising Pharma Holdings, Inc.)

NDC Code16571-412-50
Package Description500 TABLET in 1 BOTTLE (16571-412-50)
Product NDC16571-412
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20040910
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerRising Pharma Holdings, Inc.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16571-412-50





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