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"33342-322-12" National Drug Code (NDC)

Moxifloxacin 10 BLISTER PACK in 1 CARTON (33342-322-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
(Macleods Pharmaceuticals Limited)

NDC Code33342-322-12
Package Description10 BLISTER PACK in 1 CARTON (33342-322-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/33342-322-12





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