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 50 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
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)
77771-144-05 77771-144 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221026 N/A ANDA ANDA207479 RADHA PHARMACEUTICALS, INC. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-05)
77771-144-30 77771-144 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221026 N/A ANDA ANDA207479 RADHA PHARMACEUTICALS, INC. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-30)
77771-144-90 77771-144 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221026 N/A ANDA ANDA207479 RADHA PHARMACEUTICALS, INC. BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-90)
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)
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)
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)
77771-145-30 77771-145 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221026 N/A ANDA ANDA207479 RADHA PHARMACEUTICALS, INC. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-30)
77771-145-90 77771-145 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20221026 N/A ANDA ANDA207479 RADHA PHARMACEUTICALS, INC. BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-145-90)
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)
43598-656-05 43598-656 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 300 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-05)
43598-656-30 43598-656 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 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-30)
43598-656-90 43598-656 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 300 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43598-656-90)
69097-071-12 69097-071 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231025 N/A ANDA ANDA207479 Cipla USA., Inc. BUPROPION HYDROCHLORIDE 150 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-071-12)
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)
50228-145-30 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 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-145-30)
50228-145-90 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 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-145-90)
70518-3790-0 70518-3790 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20230713 N/A ANDA ANDA207479 REMEDYREPACK INC. BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-3790-0)
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)
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