"70518-1278-7" National Drug Code (NDC)

Ciprofloxacin 20 TABLET, FILM COATED in 1 BLISTER PACK (70518-1278-7)
(REMEDYREPACK INC.)

NDC Code70518-1278-7
Package Description20 TABLET, FILM COATED in 1 BLISTER PACK (70518-1278-7)
Product NDC70518-1278
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180626
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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