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=ANDA208652"
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
62135-875-30 62135-875 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE (XL) BUPROPION HYDROCHLORIDE (XL) TABLET, EXTENDED RELEASE ORAL 20240328 N/A ANDA ANDA208652 Chartwell RX, LLC BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 PACKAGE (62135-875-30)
62135-876-30 62135-876 HUMAN PRESCRIPTION DRUG BUPROPION HYDROCHLORIDE (XL) BUPROPION HYDROCHLORIDE (XL) TABLET, EXTENDED RELEASE ORAL 20240328 N/A ANDA ANDA208652 Chartwell RX, LLC BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 PACKAGE (62135-876-30)
69680-157-30 69680-157 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-30)
69680-157-90 69680-157 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-90)
69680-157-92 69680-157 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-92)
69680-157-93 69680-157 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 150 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-157-93)
69680-158-30 69680-158 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-30)
69680-158-90 69680-158 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-90)
69680-158-92 69680-158 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 300 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-92)
69680-158-93 69680-158 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20230417 N/A ANDA ANDA208652 Vitruvias Therapeutics BUPROPION HYDROCHLORIDE 300 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (69680-158-93)
71335-0824-1 71335-0824 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA208652 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-1)
71335-0824-2 71335-0824 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA208652 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-2)
71335-0824-3 71335-0824 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA208652 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-3)
71335-0824-4 71335-0824 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA208652 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-4)
71335-0824-5 71335-0824 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20180515 N/A ANDA ANDA208652 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0824-5)
0527-2415-32 0527-2415 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20220131 N/A ANDA ANDA208652 Lannett Company Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-32)
0527-2415-41 0527-2415 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20220131 N/A ANDA ANDA208652 Lannett Company Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-41)
0527-2415-43 0527-2415 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20220131 N/A ANDA ANDA208652 Lannett Company Inc. BUPROPION HYDROCHLORIDE 150 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-43)
0527-2415-46 0527-2415 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20220131 N/A ANDA ANDA208652 Lannett Company Inc. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2415-46)
0527-2430-32 0527-2430 HUMAN PRESCRIPTION DRUG Bupropion hydrochloride (XL) Bupropion hydrochloride TABLET, EXTENDED RELEASE ORAL 20220131 N/A ANDA ANDA208652 Lannett Company Inc. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0527-2430-32)
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