"50436-3135-4" National Drug Code (NDC)

Ciprofloxacin 10 TABLET in 1 BOTTLE (50436-3135-4)
(Unit Dose Services)

NDC Code50436-3135-4
Package Description10 TABLET in 1 BOTTLE (50436-3135-4)
Product NDC50436-3135
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20040910
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerUnit Dose Services
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]

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