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
70518-3251-5	70518-3251	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20230228	N/A	ANDA	ANDA213324	REMEDYREPACK INC.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-5)
70518-3251-6	70518-3251	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20250609	N/A	ANDA	ANDA213324	REMEDYREPACK INC.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-6)
85509-1415-3	85509-1415	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20251114	N/A	ANDA	ANDA213324	PHOENIX RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85509-1415-3)
85509-1415-6	85509-1415	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20251114	N/A	ANDA	ANDA213324	PHOENIX RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85509-1415-6)
85509-1415-9	85509-1415	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine hydrochloride	Cyclobenzaprine hydrochloride	TABLET, FILM COATED	ORAL	20251114	N/A	ANDA	ANDA213324	PHOENIX RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (85509-1415-9)