"52959-677-45" National Drug Code (NDC)

NDC Code	52959-677-45
Package Description	45 TABLET in 1 BOTTLE (52959-677-45)
Product NDC	52959-677
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Baclofen
Non-Proprietary Name	Baclofen
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20100715
Marketing Category Name	ANDA
Application Number	ANDA072235
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	BACLOFEN
Strength	20
Strength Unit	mg/1
Pharmacy Classes	GABA A Agonists [MoA],GABA B Agonists [MoA],gamma-Aminobutyric Acid-ergic Agonist [EPC]