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
67046-1645-3	67046-1645	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20260107	N/A	ANDA	ANDA077563	Coupler LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1645-3)
69306-872-03	69306-872	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20251031	N/A	ANDA	ANDA077563	Doc Rx	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (69306-872-03)
69306-872-06	69306-872	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20251031	N/A	ANDA	ANDA077563	Doc Rx	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (69306-872-06)
80425-0547-1	80425-0547	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250808	N/A	ANDA	ANDA077563	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0547-1)
80425-0547-2	80425-0547	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250808	N/A	ANDA	ANDA077563	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0547-2)
80425-0547-3	80425-0547	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250808	N/A	ANDA	ANDA077563	Advanced Rx of Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0547-3)
70512-872-10	70512-872	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20250731	N/A	ANDA	ANDA077563	SOLA Pharmaceuticals, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70512-872-10)