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"0093-0733-10" National Drug Code (NDC)

Metoprolol Tartrate 1000 TABLET, FILM COATED in 1 BOTTLE (0093-0733-10)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-0733-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (0093-0733-10)
Product NDC0093-0733
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date19950406
Marketing Category NameANDA
Application NumberANDA074141
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameMETOPROLOL TARTRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0093-0733-10





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