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"70518-3713-0" National Drug Code (NDC)

Moxifloxacin 7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3713-0)
(REMEDYREPACK INC.)

NDC Code70518-3713-0
Package Description7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3713-0)
Product NDC70518-3713
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMoxifloxacin
Non-Proprietary NameMoxifloxacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230412
Marketing Category NameANDA
Application NumberANDA076938
ManufacturerREMEDYREPACK INC.
Substance NameMOXIFLOXACIN HYDROCHLORIDE
Strength400
Strength Unitmg/1
Pharmacy ClassesFluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-3713-0





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