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=ANDA070184"
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
0093-2203-05 0093-2203 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 19900930 N/A ANDA ANDA070184 Teva Pharmaceuticals USA, Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 500 TABLET in 1 BOTTLE (0093-2203-05)
0093-2203-10 0093-2203 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 19900930 N/A ANDA ANDA070184 Teva Pharmaceuticals USA, Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 1000 TABLET in 1 BOTTLE (0093-2203-10)
66267-286-20 66267-286 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20161108 N/A ANDA ANDA070184 NuCare Pharmaceuticals, Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 20 TABLET in 1 BOTTLE (66267-286-20)
66267-286-30 66267-286 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20161108 N/A ANDA ANDA070184 NuCare Pharmaceuticals, Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (66267-286-30)
66267-286-60 66267-286 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20161108 N/A ANDA ANDA070184 NuCare Pharmaceuticals, Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 60 TABLET in 1 BOTTLE (66267-286-60)
66267-827-04 66267-827 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20171108 N/A ANDA ANDA070184 NuCare Pharmaceuticals,Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 4 TABLET in 1 BOTTLE (66267-827-04)
66267-827-06 66267-827 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20171108 N/A ANDA ANDA070184 NuCare Pharmaceuticals,Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 6 TABLET in 1 BOTTLE (66267-827-06)
66267-827-08 66267-827 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20171108 N/A ANDA ANDA070184 NuCare Pharmaceuticals,Inc. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 8 TABLET in 1 BOTTLE (66267-827-08)
70518-0669-0 70518-0669 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20190814 N/A ANDA ANDA070184 REMEDYREPACK INC. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BLISTER PACK (70518-0669-0)
63187-235-12 63187-235 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20230120 N/A ANDA ANDA070184 Proficient Rx LP METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 12 TABLET in 1 BOTTLE (63187-235-12)
63187-235-30 63187-235 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20141101 N/A ANDA ANDA070184 Proficient Rx LP METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 30 TABLET in 1 BOTTLE (63187-235-30)
63187-235-60 63187-235 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20141101 N/A ANDA ANDA070184 Proficient Rx LP METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 60 TABLET in 1 BOTTLE (63187-235-60)
63187-235-90 63187-235 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20141101 N/A ANDA ANDA070184 Proficient Rx LP METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 90 TABLET in 1 BOTTLE (63187-235-90)
70518-1193-0 70518-1193 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20180514 N/A ANDA ANDA070184 REMEDYREPACK INC. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (70518-1193-0)
70518-1193-4 70518-1193 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20241125 N/A ANDA ANDA070184 REMEDYREPACK INC. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (70518-1193-4)
70518-1193-5 70518-1193 HUMAN PRESCRIPTION DRUG Metoclopramide Metoclopramide TABLET ORAL 20251118 N/A ANDA ANDA070184 REMEDYREPACK INC. METOCLOPRAMIDE HYDROCHLORIDE 10 mg/1 40 TABLET in 1 BOTTLE, PLASTIC (70518-1193-5)
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