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"60687-652-21" National Drug Code (NDC)

Nebivolol 30 BLISTER PACK in 1 CARTON (60687-652-21) / 1 TABLET in 1 BLISTER PACK (60687-652-11)
(American Health Packaging)

NDC Code60687-652-21
Package Description30 BLISTER PACK in 1 CARTON (60687-652-21) / 1 TABLET in 1 BLISTER PACK (60687-652-11)
Product NDC60687-652
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20220907
Marketing Category NameANDA
Application NumberANDA203828
ManufacturerAmerican Health Packaging
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60687-652-21





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