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"70518-2341-2" National Drug Code (NDC)

Ciprofloxacin 30 TABLET, COATED in 1 BLISTER PACK (70518-2341-2)
(REMEDYREPACK INC.)

NDC Code70518-2341-2
Package Description30 TABLET, COATED in 1 BLISTER PACK (70518-2341-2)
Product NDC70518-2341
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCiprofloxacin
Non-Proprietary NameCiprofloxacin Tablets
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20191003
Marketing Category NameANDA
Application NumberANDA208921
ManufacturerREMEDYREPACK INC.
Substance NameCIPROFLOXACIN HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesQuinolone Antimicrobial [EPC],Quinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2341-2





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