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"70518-3035-3" National Drug Code (NDC)

Ciprofloxacin 14 TABLET, COATED in 1 BLISTER PACK (70518-3035-3)
(REMEDYREPACK INC.)

NDC Code70518-3035-3
Package Description14 TABLET, COATED in 1 BLISTER PACK (70518-3035-3)
Product NDC70518-3035
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20210301
Marketing Category NameANDA
Application NumberANDA208921
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/70518-3035-3





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