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=ANDA206948"
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
51655-754-20 51655-754 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20210715 N/A ANDA ANDA206948 Northwind Health Company, LLC BENZONATATE 100 mg/1 20 CAPSULE in 1 BOTTLE, PLASTIC (51655-754-20)
51655-754-21 51655-754 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20230531 N/A ANDA ANDA206948 Northwind Health Company, LLC BENZONATATE 100 mg/1 21 CAPSULE in 1 BOTTLE, PLASTIC (51655-754-21)
51655-754-52 51655-754 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20221005 N/A ANDA ANDA206948 Northwind Health Company, LLC BENZONATATE 100 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (51655-754-52)
51655-754-54 51655-754 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20221130 N/A ANDA ANDA206948 Northwind Health Company, LLC BENZONATATE 100 mg/1 15 CAPSULE in 1 BOTTLE, PLASTIC (51655-754-54)
51655-754-85 51655-754 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20231221 N/A ANDA ANDA206948 Northwind Health Company, LLC BENZONATATE 100 mg/1 9 CAPSULE in 1 BOTTLE, PLASTIC (51655-754-85)
72789-232-21 72789-232 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20220509 N/A ANDA ANDA206948 PD-Rx Pharmaceuticals, Inc. BENZONATATE 200 mg/1 21 CAPSULE in 1 BOTTLE, PLASTIC (72789-232-21)
72789-232-30 72789-232 HUMAN PRESCRIPTION DRUG Benzonatate Benzonatate CAPSULE ORAL 20220208 N/A ANDA ANDA206948 PD-Rx Pharmaceuticals, Inc. BENZONATATE 200 mg/1 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-232-30)
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