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
82868-097-96 82868-097 HUMAN PRESCRIPTION DRUG Bupropion Hydrochloride (XL) bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260112 N/A ANDA ANDA207479 Northwind Health Company, LLC BUPROPION HYDROCHLORIDE 150 mg/1 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-097-96)
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)
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)
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)
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)
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)
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