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"70518-2615-1" National Drug Code (NDC)

Metoprolol Tartrate 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2615-1)
(REMEDYREPACK INC.)

NDC Code70518-2615-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2615-1)
Product NDC70518-2615
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200309
Marketing Category NameANDA
Application NumberANDA077739
ManufacturerREMEDYREPACK INC.
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/70518-2615-1





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