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
80425-0478-1	80425-0478	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20250130	N/A	ANDA	ANDA214374	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	30 TABLET in 1 BOTTLE (80425-0478-1)
80425-0478-2	80425-0478	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20250130	N/A	ANDA	ANDA214374	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	60 TABLET in 1 BOTTLE (80425-0478-2)
80425-0478-3	80425-0478	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20250130	N/A	ANDA	ANDA214374	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	90 TABLET in 1 BOTTLE (80425-0478-3)
80425-0478-4	80425-0478	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20250130	N/A	ANDA	ANDA214374	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	120 TABLET in 1 BOTTLE (80425-0478-4)
83008-018-30	83008-018	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230425	20260228	ANDA	ANDA214374	Quality Care Products, LLC	BACLOFEN	20 mg/1	30 TABLET in 1 BOTTLE (83008-018-30)
83008-018-60	83008-018	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230425	20260228	ANDA	ANDA214374	Quality Care Products, LLC	BACLOFEN	20 mg/1	60 TABLET in 1 BOTTLE (83008-018-60)
83008-018-90	83008-018	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230425	20260228	ANDA	ANDA214374	Quality Care Products, LLC	BACLOFEN	20 mg/1	90 TABLET in 1 BOTTLE (83008-018-90)
16571-171-01	16571-171	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20240301	N/A	ANDA	ANDA214374	Rising Pharma Holdings, Inc.	BACLOFEN	10 mg/1	100 TABLET in 1 BOTTLE (16571-171-01)
16571-171-10	16571-171	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20240301	N/A	ANDA	ANDA214374	Rising Pharma Holdings, Inc.	BACLOFEN	10 mg/1	1000 TABLET in 1 BOTTLE (16571-171-10)
16571-171-50	16571-171	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20240301	N/A	ANDA	ANDA214374	Rising Pharma Holdings, Inc.	BACLOFEN	10 mg/1	500 TABLET in 1 BOTTLE (16571-171-50)
68071-3700-3	68071-3700	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20241022	N/A	ANDA	ANDA214374	NuCare Pharmaceuticals, Inc.	BACLOFEN	10 mg/1	30 TABLET in 1 BOTTLE (68071-3700-3)
68071-3700-6	68071-3700	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20241029	N/A	ANDA	ANDA214374	NuCare Pharmaceuticals, Inc.	BACLOFEN	10 mg/1	60 TABLET in 1 BOTTLE (68071-3700-6)
68071-3700-9	68071-3700	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20241022	N/A	ANDA	ANDA214374	NuCare Pharmaceuticals, Inc.	BACLOFEN	10 mg/1	90 TABLET in 1 BOTTLE (68071-3700-9)
70518-4384-0	70518-4384	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20250703	N/A	ANDA	ANDA214374	REMEDYREPACK INC.	BACLOFEN	10 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-4384-0)
16571-172-01	16571-172	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20240301	N/A	ANDA	ANDA214374	Rising Pharma Holdings, Inc.	BACLOFEN	20 mg/1	100 TABLET in 1 BOTTLE (16571-172-01)
16571-172-10	16571-172	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20240301	N/A	ANDA	ANDA214374	Rising Pharma Holdings, Inc.	BACLOFEN	20 mg/1	1000 TABLET in 1 BOTTLE (16571-172-10)
16571-172-50	16571-172	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20240301	N/A	ANDA	ANDA214374	Rising Pharma Holdings, Inc.	BACLOFEN	20 mg/1	500 TABLET in 1 BOTTLE (16571-172-50)
71335-9759-0	71335-9759	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230811	N/A	ANDA	ANDA214374	Bryant Ranch Prepack	BACLOFEN	10 mg/1	112 TABLET in 1 BOTTLE (71335-9759-0)
71335-9759-1	71335-9759	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230811	N/A	ANDA	ANDA214374	Bryant Ranch Prepack	BACLOFEN	10 mg/1	30 TABLET in 1 BOTTLE (71335-9759-1)
71335-9759-2	71335-9759	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230811	N/A	ANDA	ANDA214374	Bryant Ranch Prepack	BACLOFEN	10 mg/1	120 TABLET in 1 BOTTLE (71335-9759-2)