"42291-142-45" National Drug Code (NDC)

NDC Code	42291-142-45
Package Description	45 TABLET in 1 BOTTLE (42291-142-45)
Product NDC	42291-142
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Atenolol
Non-Proprietary Name	Atenolol
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130617
Marketing Category Name	ANDA
Application Number	ANDA074056
Manufacturer	AvKARE, Inc.
Substance Name	ATENOLOL
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]