"68071-3337-1" National Drug Code (NDC)

Metoprolol Tartrate 120 TABLET, FILM COATED in 1 BOTTLE (68071-3337-1)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-3337-1
Package Description120 TABLET, FILM COATED in 1 BOTTLE (68071-3337-1)
Product NDC68071-3337
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMetoprolol Tartrate
Non-Proprietary NameMetoprolol Tartrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070911
Marketing Category NameANDA
Application NumberANDA077739
ManufacturerNuCare Pharmaceuticals, Inc.
Substance NameMETOPROLOL TARTRATE
Strength50
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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