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=ANDA207479"
符合检索条件的记录共 51 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
69097-072-12 69097-072 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231025 N/A ANDA ANDA207479 Cipla USA., Inc. BUPROPION HYDROCHLORIDE 300 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-072-12)
43598-655-90 43598-655 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Dr Reddys Laboratories Inc BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-655-90)
63629-8474-1 63629-8474 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8474-1)
63629-8475-1 63629-8475 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8475-1)
63629-8476-1 63629-8476 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63629-8476-1)
43598-655-05 43598-655 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Dr Reddys Laboratories Inc BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-655-05)
43598-655-30 43598-655 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Dr Reddys Laboratories Inc BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-655-30)
83008-082-30 83008-082 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240828 20261231 ANDA ANDA207479 Quality Care Products, LLC BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83008-082-30)
50228-145-05 50228-145 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 ScieGen Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 300 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-145-05)
50228-144-30 50228-144 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 ScieGen Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-30)
50228-144-90 50228-144 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 ScieGen Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-90)
70518-3790-1 70518-3790 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20240607 N/A ANDA ANDA207479 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3790-1)
70518-3790-2 70518-3790 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260320 N/A ANDA ANDA207479 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3790-2)
70518-3790-3 70518-3790 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260415 N/A ANDA ANDA207479 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3790-3)
80425-0539-1 80425-0539 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250829 N/A ANDA ANDA207479 Advanced Rx of Tennessee, LLC BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-1)
80425-0539-2 80425-0539 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250829 N/A ANDA ANDA207479 Advanced Rx of Tennessee, LLC BUPROPION HYDROCHLORIDE 300 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-2)
80425-0539-3 80425-0539 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250829 N/A ANDA ANDA207479 Advanced Rx of Tennessee, LLC BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (80425-0539-3)
72162-1526-3 72162-1526 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1526-3)
72162-1526-5 72162-1526 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1526-5)
50228-144-05 50228-144 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20170412 N/A ANDA ANDA207479 ScieGen Pharmaceuticals,Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-144-05)
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