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"13107-064-99" National Drug Code (NDC)

Metoprolol Tartrate 1000 TABLET, FILM COATED in 1 BOTTLE (13107-064-99)
(Aurolife Pharma LLC)

NDC Code13107-064-99
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (13107-064-99)
Product NDC13107-064
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100917
Marketing Category NameANDA
Application NumberANDA077739
ManufacturerAurolife Pharma LLC
Substance NameMETOPROLOL TARTRATE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/13107-064-99





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