"68001-502-03" National Drug Code (NDC)

Metoprolol Succinate 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-502-03)
(BluePoint Laboratories)

NDC Code68001-502-03
Package Description500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-502-03)
Product NDC68001-502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Succinate
Non-Proprietary NameMetoprolol Succinate Er Tablets
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20210514
Marketing Category NameANDA
Application NumberANDA211143
ManufacturerBluePoint Laboratories
Substance NameMETOPROLOL SUCCINATE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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