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"71335-2502-7" National Drug Code (NDC)

Ciprofloxacin 12 TABLET in 1 BOTTLE (71335-2502-7)
(Bryant Ranch Prepack)

NDC Code71335-2502-7
Package Description12 TABLET in 1 BOTTLE (71335-2502-7)
Product NDC71335-2502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofolxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20231001
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerBryant Ranch Prepack
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
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/71335-2502-7





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