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"
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
50090-7335-0 50090-7335 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20241015 N/A ANDA ANDA207479 A-S Medication Solutions BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7335-0)
50090-7334-1 50090-7334 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20241015 N/A ANDA ANDA207479 A-S Medication Solutions BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-1)
50090-7334-0 50090-7334 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20241015 N/A ANDA ANDA207479 A-S Medication Solutions BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7334-0)
71335-2312-1 71335-2312 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231221 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-1)
71335-2312-5 71335-2312 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231221 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 8 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-5)
71335-2312-6 71335-2312 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231221 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-6)
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)
71335-2312-2 71335-2312 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231221 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-2)
71335-2312-3 71335-2312 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231221 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-3)
71335-2312-4 71335-2312 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231221 N/A ANDA ANDA207479 Bryant Ranch Prepack BUPROPION HYDROCHLORIDE 300 mg/1 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71335-2312-4)
72162-1527-3 72162-1527 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 (72162-1527-3)
72162-1527-5 72162-1527 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 (72162-1527-5)
50090-7712-0 50090-7712 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20251014 N/A ANDA ANDA207479 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7712-0)
50090-7711-0 50090-7711 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20251014 N/A ANDA ANDA207479 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7711-0)
50090-7711-1 50090-7711 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20251014 N/A ANDA ANDA207479 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7711-1)
50090-7711-2 50090-7711 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride Bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20251014 N/A ANDA ANDA207479 A-S Medication Solutions BUPROPION HYDROCHLORIDE 150 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7711-2)
68071-3927-3 68071-3927 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20251210 N/A ANDA ANDA207479 NuCare Pharmaceuticals, Inc. BUPROPION HYDROCHLORIDE 150 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-3927-3)
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)
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