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"70518-0368-1" National Drug Code (NDC)

Ciprofloxacin 20 TABLET in 1 BOTTLE, PLASTIC (70518-0368-1)
(REMEDYREPACK INC.)

NDC Code70518-0368-1
Package Description20 TABLET in 1 BOTTLE, PLASTIC (70518-0368-1)
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 ClassesCytochrome P450 1A2 Inhibitors [MoA], Fluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-0368-1





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