"70518-2341-3" National Drug Code (NDC)

Ciprofloxacin 14 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2341-3)
(REMEDYREPACK INC.)

NDC Code70518-2341-3
Package Description14 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-2341-3)
Product NDC70518-2341
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Tablets
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20191003
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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