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"71335-0517-7" National Drug Code (NDC)

Metoprolol Tartrate 20 TABLET, FILM COATED in 1 BOTTLE (71335-0517-7)
(Bryant Ranch Prepack)

NDC Code71335-0517-7
Package Description20 TABLET, FILM COATED in 1 BOTTLE (71335-0517-7)
Product NDC71335-0517
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070911
Marketing Category NameANDA
Application NumberANDA077739
ManufacturerBryant Ranch Prepack
Substance NameMETOPROLOL TARTRATE
Strength25
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0517-7





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