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
71335-2219-0	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	120 TABLET in 1 BOTTLE (71335-2219-0)
71335-2219-1	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	90 TABLET in 1 BOTTLE (71335-2219-1)
71335-2219-2	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	20 TABLET in 1 BOTTLE (71335-2219-2)
71335-2219-3	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	60 TABLET in 1 BOTTLE (71335-2219-3)
71335-2219-4	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	45 TABLET in 1 BOTTLE (71335-2219-4)
71335-2219-5	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	112 TABLET in 1 BOTTLE (71335-2219-5)
71335-2219-6	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	30 TABLET in 1 BOTTLE (71335-2219-6)
71335-2219-7	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	56 TABLET in 1 BOTTLE (71335-2219-7)
71335-2219-8	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	15 TABLET in 1 BOTTLE (71335-2219-8)
71335-2219-9	71335-2219	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230815	N/A	ANDA	ANDA214099	Bryant Ranch Prepack	BACLOFEN	20 mg/1	84 TABLET in 1 BOTTLE (71335-2219-9)
70518-3467-2	70518-3467	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20220928	N/A	ANDA	ANDA214099	REMEDYREPACK INC.	BACLOFEN	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3467-2)
70518-3467-0	70518-3467	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20220805	N/A	ANDA	ANDA214099	REMEDYREPACK INC.	BACLOFEN	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-3467-0)
84386-035-01	84386-035	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20251121	N/A	ANDA	ANDA214099	Aurobindo Pharma Limited	BACLOFEN	5 mg/1	100 TABLET in 1 BOTTLE (84386-035-01)
85534-0004-0	85534-0004	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20250611	N/A	ANDA	ANDA214099	HAWAII REPACK, INC.	BACLOFEN	20 mg/1	100 TABLET in 1 BOTTLE (85534-0004-0)
85534-0004-9	85534-0004	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20250611	N/A	ANDA	ANDA214099	HAWAII REPACK, INC.	BACLOFEN	20 mg/1	90 TABLET in 1 BOTTLE (85534-0004-9)
68071-3407-3	68071-3407	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20230531	N/A	ANDA	ANDA214099	NuCare Pharmaceuticals,Inc.	BACLOFEN	10 mg/1	3 TABLET in 1 BOTTLE (68071-3407-3)
80425-0466-1	80425-0466	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20241228	N/A	ANDA	ANDA214099	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	30 TABLET in 1 BOTTLE (80425-0466-1)
80425-0466-2	80425-0466	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20241228	N/A	ANDA	ANDA214099	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	60 TABLET in 1 BOTTLE (80425-0466-2)
80425-0466-3	80425-0466	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20241228	N/A	ANDA	ANDA214099	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	90 TABLET in 1 BOTTLE (80425-0466-3)
80425-0466-4	80425-0466	HUMAN PRESCRIPTION DRUG	BACLOFEN	BACLOFEN	TABLET	ORAL	20241228	N/A	ANDA	ANDA214099	Advanced Rx of Tennessee, LLC	BACLOFEN	20 mg/1	120 TABLET in 1 BOTTLE (80425-0466-4)