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=ANDA076264"
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
68084-291-21 68084-291 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20121206 N/A ANDA ANDA076264 American Health Packaging NALTREXONE HYDROCHLORIDE 50 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11)
72162-2154-3 72162-2154 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20231207 N/A ANDA ANDA076264 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72162-2154-3)
50090-6820-0 50090-6820 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20231114 N/A ANDA ANDA076264 A-S Medication Solutions NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6820-0)
0406-1170-01 0406-1170 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 SpecGx LLC NALTREXONE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01)
0406-1170-03 0406-1170 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 SpecGx LLC NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03)
71335-1480-1 71335-1480 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1480-1)
71335-1480-2 71335-1480 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1480-2)
71335-1480-3 71335-1480 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-1480-3)
71335-1480-4 71335-1480 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71335-1480-4)
71335-1480-5 71335-1480 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1480-5)
71335-1480-6 71335-1480 HUMAN PRESCRIPTION DRUG NALTREXONE HYDROCHLORIDE naltrexone hydrochloride TABLET, FILM COATED ORAL 20020322 N/A ANDA ANDA076264 Bryant Ranch Prepack NALTREXONE HYDROCHLORIDE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-1480-6)
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