"68788-7192-3" National Drug Code (NDC)

Metoprolol Tartrate 30 TABLET, FILM COATED in 1 BOTTLE (68788-7192-3)
(Preferred Pharmaceuticals, Inc.)

NDC Code68788-7192-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68788-7192-3)
Product NDC68788-7192
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20180718
Marketing Category NameANDA
Application NumberANDA200981
ManufacturerPreferred Pharmaceuticals, Inc.
Substance NameMETOPROLOL TARTRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

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