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"70518-0381-2" National Drug Code (NDC)

Metoprolol Tartrate 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0381-2)
(REMEDYREPACK INC.)

NDC Code70518-0381-2
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0381-2)
Product NDC70518-0381
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170403
Marketing Category NameANDA
Application NumberANDA076704
ManufacturerREMEDYREPACK 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/70518-0381-2





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