美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
63629-9689-1	63629-9689	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20230621	N/A	ANDA	ANDA207138	Bryant Ranch Prepack	OXYBUTYNIN CHLORIDE	5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9689-1)
63629-9689-2	63629-9689	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20230621	N/A	ANDA	ANDA207138	Bryant Ranch Prepack	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-9689-2)
72789-049-90	72789-049	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20200128	N/A	ANDA	ANDA207138	PD-Rx Pharmaceuticals, Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-049-90)
72189-131-30	72189-131	HUMAN PRESCRIPTION DRUG	OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20201111	N/A	ANDA	ANDA207138	direct rx	OXYBUTYNIN CHLORIDE	5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-131-30)
72189-132-30	72189-132	HUMAN PRESCRIPTION DRUG	OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200824	N/A	ANDA	ANDA207138	DIRECT RX	OXYBUTYNIN CHLORIDE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-132-30)
50090-5822-1	50090-5822	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20230719	N/A	ANDA	ANDA207138	A-S Medication Solutions	OXYBUTYNIN CHLORIDE	5 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-1)
50090-5822-0	50090-5822	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20211020	N/A	ANDA	ANDA207138	A-S Medication Solutions	OXYBUTYNIN CHLORIDE	5 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-5822-0)
50090-4307-0	50090-4307	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20190523	N/A	ANDA	ANDA207138	A-S Medication Solutions	OXYBUTYNIN CHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-4307-0)
71205-667-30	71205-667	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20220608	N/A	ANDA	ANDA207138	Proficient Rx LP	OXYBUTYNIN CHLORIDE	10 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-30)
71205-667-60	71205-667	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20220608	N/A	ANDA	ANDA207138	Proficient Rx LP	OXYBUTYNIN CHLORIDE	10 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60)
71205-667-90	71205-667	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20220608	N/A	ANDA	ANDA207138	Proficient Rx LP	OXYBUTYNIN CHLORIDE	10 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90)
16729-317-16	16729-317	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20170330	N/A	ANDA	ANDA207138	Accord Healthcare, Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-317-16)
16729-319-01	16729-319	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20161214	N/A	ANDA	ANDA207138	Accord Healthcare, Inc.	OXYBUTYNIN CHLORIDE	15 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-319-01)
16729-318-01	16729-318	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20161220	N/A	ANDA	ANDA207138	Accord Healthcare, Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-318-01)
16729-318-16	16729-318	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20170417	N/A	ANDA	ANDA207138	Accord Healthcare, Inc.	OXYBUTYNIN CHLORIDE	10 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-318-16)
16729-317-01	16729-317	HUMAN PRESCRIPTION DRUG	oxybutynin chloride	oxybutynin chloride	TABLET, EXTENDED RELEASE	ORAL	20161214	N/A	ANDA	ANDA207138	Accord Healthcare, Inc.	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-317-01)