"70518-1090-0" National Drug Code (NDC)

Ciprofloxacin 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1090-0)
(REMEDYREPACK INC.)

NDC Code70518-1090-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1090-0)
Product NDC70518-1090
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180402
Marketing Category NameANDA
Application NumberANDA075593
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength250
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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