"70518-2837-1" National Drug Code (NDC)

Ciprofloxacin 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-1)
(REMEDYREPACK INC.)

NDC Code70518-2837-1
Package Description10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-1)
Product NDC70518-2837
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200818
Marketing Category NameANDA
Application NumberANDA076558
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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