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=ANDA090478"
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
50268-190-15 50268-190 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20140610 N/A ANDA ANDA090478 AvPAK CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 50 BLISTER PACK in 1 BOX (50268-190-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-190-11)
69097-845-07 69097-845 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20160722 N/A ANDA ANDA090478 Cipla USA Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69097-845-07)
69097-845-15 69097-845 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20160722 N/A ANDA ANDA090478 Cipla USA Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69097-845-15)
60687-558-01 60687-558 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220210 N/A ANDA ANDA090478 American Health Packaging CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 BLISTER PACK in 1 CARTON (60687-558-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-558-11)
69097-846-07 69097-846 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20160722 N/A ANDA ANDA090478 Cipla USA Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69097-846-07)
69097-846-15 69097-846 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20160722 N/A ANDA ANDA090478 Cipla USA Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69097-846-15)
51655-973-20 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20221017 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-20)
51655-973-25 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220906 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-25)
51655-973-52 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20221007 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-52)
51655-973-53 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220727 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-53)
51655-973-54 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220824 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-54)
51655-973-87 51655-973 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20220504 N/A ANDA ANDA090478 Northwind Health Company, LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-973-87)
76282-283-10 76282-283 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET ORAL 20250410 N/A ANDA ANDA090478 EXELAN PHARMACEUTICALS, INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (76282-283-10)
63187-812-07 63187-812 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20210514 N/A ANDA ANDA090478 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (63187-812-07)
63187-812-10 63187-812 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20170801 N/A ANDA ANDA090478 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (63187-812-10)
63187-812-12 63187-812 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20180402 N/A ANDA ANDA090478 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (63187-812-12)
63187-812-15 63187-812 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20170202 N/A ANDA ANDA090478 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (63187-812-15)
63187-812-20 63187-812 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20170202 N/A ANDA ANDA090478 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (63187-812-20)
63187-812-21 63187-812 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA090478 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (63187-812-21)
63187-812-30 63187-812 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine TABLET, FILM COATED ORAL 20170201 N/A ANDA ANDA090478 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-812-30)
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