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"71335-0339-7" National Drug Code (NDC)

Ciprofloxacin 90 TABLET in 1 BOTTLE (71335-0339-7)
(Bryant Ranch Prepack)

NDC Code71335-0339-7
Package Description90 TABLET in 1 BOTTLE (71335-0339-7)
Product NDC71335-0339
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20040910
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerBryant Ranch Prepack
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength750
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0339-7





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