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"71335-2329-1" National Drug Code (NDC)

Moxifloxacin Hydrochloride 7 TABLET, FILM COATED in 1 BOTTLE (71335-2329-1)
(Bryant Ranch Prepack)

NDC Code71335-2329-1
Package Description7 TABLET, FILM COATED in 1 BOTTLE (71335-2329-1)
Product NDC71335-2329
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMoxifloxacin Hydrochloride
Non-Proprietary NameMoxifloxacin Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140304
Marketing Category NameANDA
Application NumberANDA202632
ManufacturerBryant Ranch Prepack
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/71335-2329-1





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