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"50436-3135-3" National Drug Code (NDC)

Ciprofloxacin 21 TABLET in 1 BOTTLE (50436-3135-3)
(Unit Dose Services)

NDC Code50436-3135-3
Package Description21 TABLET in 1 BOTTLE (50436-3135-3)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50436-3135-3





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