"31722-585-32" National Drug Code (NDC)

Nebivolol 12 BLISTER PACK in 1 CARTON (31722-585-32) / 10 TABLET in 1 BLISTER PACK (31722-585-31)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-585-32
Package Description12 BLISTER PACK in 1 CARTON (31722-585-32) / 10 TABLET in 1 BLISTER PACK (31722-585-31)
Product NDC31722-585
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameNebivolol
Non-Proprietary NameNebivolol
Dosage FormTABLET
UsageORAL
Start Marketing Date20210917
Marketing Category NameANDA
Application NumberANDA203825
ManufacturerCamber Pharmaceuticals, Inc.
Substance NameNEBIVOLOL HYDROCHLORIDE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesAdrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]

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