"70095-019-01" National Drug Code (NDC)

Bisoprolol Fumarate 30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-019-01)
(Sun Pharmaceutical Industries Limited)

NDC Code70095-019-01
Package Description30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-019-01)
Product NDC70095-019
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBisoprolol Fumarate
Non-Proprietary NameBisoprolol Fumarate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240310
Marketing Category NameANDA
Application NumberANDA217617
ManufacturerSun Pharmaceutical Industries Limited
Substance NameBISOPROLOL FUMARATE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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