"70518-0368-2" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BLISTER PACK (70518-0368-2)
(REMEDYREPACK INC.)

NDC Code70518-0368-2
Package Description20 TABLET in 1 BLISTER PACK (70518-0368-2)
Product NDC70518-0368
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET
UsageORAL
Start Marketing Date20170329
Marketing Category NameANDA
Application NumberANDA076639
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC], Quinolones [CS]

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