"52343-061-99" National Drug Code (NDC)

Metoprolol Tartrate 1000 TABLET, FILM COATED in 1 BOTTLE (52343-061-99)
(ACETRIS HEALTH, LLC)

NDC Code52343-061-99
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (52343-061-99)
Product NDC52343-061
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
ManufacturerACETRIS HEALTH, LLC
Substance NameMETOPROLOL TARTRATE
Strength100
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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