"60687-679-21" National Drug Code (NDC)

Bisoprolol Fumarate 30 BLISTER PACK in 1 CARTON (60687-679-21) / 1 TABLET in 1 BLISTER PACK (60687-679-11)
(American Health Packaging)

NDC Code60687-679-21
Package Description30 BLISTER PACK in 1 CARTON (60687-679-21) / 1 TABLET in 1 BLISTER PACK (60687-679-11)
Product NDC60687-679
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBisoprolol Fumarate
Non-Proprietary NameBisoprolol Fumarate
Dosage FormTABLET
UsageORAL
Start Marketing Date20230420
Marketing Category NameANDA
Application NumberANDA078635
ManufacturerAmerican Health Packaging
Substance NameBISOPROLOL FUMARATE
Strength5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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