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
43063-532-14 43063-532 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20140630 N/A ANDA ANDA091680 PD-Rx Pharmaceuticals, Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-14)
43063-532-21 43063-532 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20171219 N/A ANDA ANDA091680 PD-Rx Pharmaceuticals, Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 21 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-21)
43063-532-28 43063-532 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20161114 N/A ANDA ANDA091680 PD-Rx Pharmaceuticals, Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-28)
43063-532-30 43063-532 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20140725 N/A ANDA ANDA091680 PD-Rx Pharmaceuticals, Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-30)
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)
71335-0049-1 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 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0049-1)
68071-3837-1 68071-3837 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20250421 N/A ANDA ANDA091680 NuCare Pharmaceuticals, Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3837-1)
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)
17224-760-30 17224-760 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111024 N/A ANDA ANDA091680 Calvin Scott & Co., Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (17224-760-30)
17224-760-84 17224-760 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111024 N/A ANDA ANDA091680 Calvin Scott & Co., Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 84 TABLET, EXTENDED RELEASE in 1 BOTTLE (17224-760-84)
17224-760-56 17224-760 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111024 N/A ANDA ANDA091680 Calvin Scott & Co., Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 56 TABLET, EXTENDED RELEASE in 1 BOTTLE (17224-760-56)
17224-760-07 17224-760 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111024 N/A ANDA ANDA091680 Calvin Scott & Co., Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (17224-760-07)
17224-760-28 17224-760 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER DIETHYLPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20111024 N/A ANDA ANDA091680 Calvin Scott & Co., Inc. DIETHYLPROPION HYDROCHLORIDE 75 mg/1 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (17224-760-28)
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