"70518-3417-2" National Drug Code (NDC)

Ciprofloxacin 20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-2)
(REMEDYREPACK INC.)

NDC Code70518-3417-2
Package Description20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3417-2)
Product NDC70518-3417
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20220511
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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