"70518-4214-1" National Drug Code (NDC)

Ciprofloxacin 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)
(REMEDYREPACK INC.)

NDC Code70518-4214-1
Package Description14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4214-1)
Product NDC70518-4214
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20241015
Marketing Category NameANDA
Application NumberANDA077859
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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