"52959-527-20" National Drug Code (NDC)

NDC Code	52959-527-20
Package Description	20 TABLET, EXTENDED RELEASE in 1 BOTTLE (52959-527-20)
Product NDC	52959-527
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Orphenadrine Citrate
Non-Proprietary Name	Orphenadrine Citrate
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20000623
Marketing Category Name	ANDA
Application Number	ANDA040368
Manufacturer	H.J. Harkins Company, Inc.
Substance Name	ORPHENADRINE CITRATE
Strength	100
Strength Unit	mg/1
Pharmacy Classes	Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]