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
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)
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)
43063-532-07 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 7 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-532-07)
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)
63187-621-30 63187-621 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20160101 N/A ANDA ANDA091680 Proficient Rx LP DIETHYLPROPION HYDROCHLORIDE 75 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-621-30)
63187-621-60 63187-621 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20160101 N/A ANDA ANDA091680 Proficient Rx LP DIETHYLPROPION HYDROCHLORIDE 75 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-621-60)
63187-621-90 63187-621 HUMAN PRESCRIPTION DRUG Diethylpropion Hydrochloride ER Diethylpropion Hydrochloride TABLET, EXTENDED RELEASE ORAL 20160101 N/A ANDA ANDA091680 Proficient Rx LP DIETHYLPROPION HYDROCHLORIDE 75 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-621-90)
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)
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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