"33342-322-07" National Drug Code (NDC)

Moxifloxacin 30 TABLET, FILM COATED in 1 BOTTLE (33342-322-07)
(Macleods Pharmaceuticals Limited)

NDC Code33342-322-07
Package Description30 TABLET, FILM COATED in 1 BOTTLE (33342-322-07)
Product NDC33342-322
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMoxifloxacin
Non-Proprietary NameMoxifloxacin
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260302
Marketing Category NameANDA
Application NumberANDA209143
ManufacturerMacleods Pharmaceuticals Limited
Substance NameMOXIFLOXACIN HYDROCHLORIDE
Strength400
Strength Unitmg/1
Pharmacy ClassesFluoroquinolone Antibacterial [EPC], Fluoroquinolones [CS]

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