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)
检索条件:" 注册申请号=ANDA208170"
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
76420-456-20 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (76420-456-20)
76420-456-30 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-456-30)
76420-456-50 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-456-50)
76420-456-60 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-456-60)
76420-456-90 76420-456 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250813 N/A ANDA ANDA208170 ASCLEMED USA INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-456-90)
72603-310-01 72603-310 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72603-310-01)
72603-310-02 72603-310 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72603-310-02)
72603-311-01 72603-311 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72603-311-01)
72603-312-01 72603-312 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72603-312-01)
72603-312-02 72603-312 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72603-312-02)
72603-312-03 72603-312 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241101 N/A ANDA ANDA208170 NORTHSTAR RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72603-312-03)
71205-356-15 71205-356 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20210720 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71205-356-15)
71205-356-20 71205-356 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230406 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-356-20)
71205-356-21 71205-356 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230406 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71205-356-21)
71205-356-30 71205-356 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-356-30)
71205-356-40 71205-356 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240108 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71205-356-40)
71205-356-60 71205-356 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-356-60)
71205-356-90 71205-356 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20191101 N/A ANDA ANDA208170 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-356-90)
70518-2611-3 70518-2611 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20241002 N/A ANDA ANDA208170 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-3)
70518-2611-4 70518-2611 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20241108 N/A ANDA ANDA208170 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2611-4)
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