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=ANDA091680"
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
71335-0049-2 71335-0049 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20120412 N/A ANDA ANDA091680 Bryant Ranch Prepack DIETHYLPROPION HYDROCHLORIDE 75 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-2)
71335-0049-3 71335-0049 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20120412 N/A ANDA ANDA091680 Bryant Ranch Prepack DIETHYLPROPION HYDROCHLORIDE 75 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-3)
71335-0049-4 71335-0049 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20120412 N/A ANDA ANDA091680 Bryant Ranch Prepack DIETHYLPROPION HYDROCHLORIDE 75 mg/1 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-4)
50090-0120-0 50090-0120 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20141128 N/A ANDA ANDA091680 A-S Medication Solutions DIETHYLPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-0120-0)
50090-0120-1 50090-0120 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20141128 N/A ANDA ANDA091680 A-S Medication Solutions DIETHYLPROPION HYDROCHLORIDE 75 mg/1 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-0120-1)
50090-0120-4 50090-0120 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20141128 N/A ANDA ANDA091680 A-S Medication Solutions DIETHYLPROPION HYDROCHLORIDE 75 mg/1 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-0120-4)
50090-0120-5 50090-0120 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20180726 N/A ANDA ANDA091680 A-S Medication Solutions DIETHYLPROPION HYDROCHLORIDE 75 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-0120-5)
81665-109-10 81665-109 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250919 N/A ANDA ANDA091680 OMNIVIUM PHARMACEUTICALS LLC. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-109-10)
81665-109-25 81665-109 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250919 N/A ANDA ANDA091680 OMNIVIUM PHARMACEUTICALS LLC. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-109-25)
0527-1477-01 0527-1477 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20111024 N/A ANDA ANDA091680 Lannett Company, Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-1477-01)
0527-1477-25 0527-1477 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20111024 N/A ANDA ANDA091680 Lannett Company, Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 250 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-1477-25)
62135-489-30 62135-489 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20230403 N/A ANDA ANDA091680 Chartwell RX, LLC. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62135-489-30)
72189-307-30 72189-307 HUMAN PRESCRIPTION DRUG DIETHYLPROPION HYDROCHLORIDE ER DIETHYLPROPION HYDROCHLORIDE ER TABLET, EXTENDED RELEASE ORAL 20211229 N/A ANDA ANDA091680 Directrx DIETHYLPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-307-30)
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