"42291-540-50" National Drug Code (NDC)

NDC Code	42291-540-50
Package Description	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-540-50)
Product NDC	42291-540
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Oxybutynin Chloride
Non-Proprietary Name	Oxybutynin Chloride
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20160108
Marketing Category Name	ANDA
Application Number	ANDA204010
Manufacturer	AvKARE, Inc.
Substance Name	OXYBUTYNIN CHLORIDE
Strength	5
Strength Unit	mg/1
Pharmacy Classes	Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]