"69367-387-50" National Drug Code (NDC)

Ciprofloxacin Hydrochloride 50 TABLET, FILM COATED in 1 BOTTLE (69367-387-50)
(Westminster Pharmaceuticals, LLC)

NDC Code69367-387-50
Package Description50 TABLET, FILM COATED in 1 BOTTLE (69367-387-50)
Product NDC69367-387
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin Hydrochloride
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240523
Marketing Category NameANDA
Application NumberANDA076593
ManufacturerWestminster Pharmaceuticals, LLC
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength750
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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