"78670-100-01" National Drug Code (NDC)

NDC Code	78670-100-01
Package Description	100 TABLET in 1 BOTTLE (78670-100-01)
Product NDC	78670-100
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Corgard
Non-Proprietary Name	Nadolol
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20220201
End Marketing Date	20240930
Marketing Category Name	NDA
Application Number	NDA018063
Manufacturer	USWM, LLC
Substance Name	NADOLOL
Strength	20
Strength Unit	mg/1
Pharmacy Classes	Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]