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
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)
60760-536-30 60760-536 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220615 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-536-30)
60760-536-90 60760-536 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230314 N/A ANDA ANDA078643 St Mary's Medical Park Pharmacy CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-536-90)
71335-2678-1 71335-2678 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20250911 N/A ANDA ANDA078643 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (71335-2678-1)
0904-7400-04 0904-7400 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 20270131 ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 BLISTER PACK in 1 CARTON (0904-7400-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7400-06 0904-7400 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 20270131 ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 50 BLISTER PACK in 1 CARTON (0904-7400-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-7401-61 0904-7401 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240221 N/A ANDA ANDA078643 Major Pharmaceuticals CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 BLISTER PACK in 1 CARTON (0904-7401-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
82868-008-30 82868-008 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240429 N/A ANDA ANDA078643 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-008-30)
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)
16571-783-50 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/1 500 TABLET, FILM COATED in 1 BOTTLE (16571-783-50)
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)
42708-172-20 42708-172 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230519 N/A ANDA ANDA078643 QPharma Inc CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-172-20)
55154-0190-0 55154-0190 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20251010 N/A ANDA ANDA078643 Cardinal Health 107, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 BLISTER PACK in 1 BAG (55154-0190-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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