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=ANDA078643"
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
68071-2659-3 68071-2659 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220328 N/A ANDA ANDA078643 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-2659-3)
68071-2659-5 68071-2659 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220328 N/A ANDA ANDA078643 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68071-2659-5)
68071-2659-6 68071-2659 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241014 N/A ANDA ANDA078643 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 6 TABLET, FILM COATED in 1 BOTTLE (68071-2659-6)
68071-2659-7 68071-2659 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20241202 N/A ANDA ANDA078643 NuCare Pharmaceuticals,Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-2659-7)
68788-8221-2 68788-8221 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220909 N/A ANDA ANDA078643 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-8221-2)
68788-8221-3 68788-8221 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220909 N/A ANDA ANDA078643 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8221-3)
68788-8221-6 68788-8221 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220909 N/A ANDA ANDA078643 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8221-6)
68788-8221-8 68788-8221 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220909 N/A ANDA ANDA078643 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-8221-8)
68788-8221-9 68788-8221 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220909 N/A ANDA ANDA078643 Preferred Pharmaceuticals Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8221-9)
16571-782-01 16571-782 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16571-782-01)
16571-782-10 16571-782 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-782-10)
16571-782-50 16571-782 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16571-782-50)
60760-889-04 60760-889 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220517 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-889-04)
60760-889-15 60760-889 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220517 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-889-15)
60760-889-20 60760-889 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220917 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-889-20)
60760-889-30 60760-889 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220517 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-889-30)
60760-889-40 60760-889 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20221130 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-889-40)
60760-889-90 60760-889 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220517 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-889-90)
16571-783-01 16571-783 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16571-783-01)
16571-783-10 16571-783 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20080926 N/A ANDA ANDA078643 Rising Pharma Holdings, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-783-10)
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