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=ANDA075797"
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
51407-440-30 51407-440 HUMAN PRESCRIPTION DRUG Tamoxifen Citrate Tamoxifen Citrate TABLET, FILM COATED ORAL 20210802 N/A ANDA ANDA075797 Golden State Medical Supply, Inc. TAMOXIFEN CITRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (51407-440-30)
63739-143-10 63739-143 HUMAN PRESCRIPTION DRUG Tamoxifen Citrate Tamoxifen Citrate TABLET, FILM COATED ORAL 20211214 N/A ANDA ANDA075797 McKesson Corporation dba SKY Packaging TAMOXIFEN CITRATE 10 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-143-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
51407-439-60 51407-439 HUMAN PRESCRIPTION DRUG Tamoxifen Citrate Tamoxifen Citrate TABLET, FILM COATED ORAL 20210802 N/A ANDA ANDA075797 Golden State Medical Supply, Inc. TAMOXIFEN CITRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (51407-439-60)
51862-643-10 51862-643 HUMAN PRESCRIPTION DRUG Tamoxifen Citrate Tamoxifen Citrate TABLET, FILM COATED ORAL 20210827 N/A ANDA ANDA075797 Mayne Pharma Commercial LLC TAMOXIFEN CITRATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (51862-643-10)
51862-642-60 51862-642 HUMAN PRESCRIPTION DRUG Tamoxifen Citrate Tamoxifen Citrate TABLET, FILM COATED ORAL 20210827 N/A ANDA ANDA075797 Mayne Pharma Commercial LLC TAMOXIFEN CITRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (51862-642-60)
51862-642-10 51862-642 HUMAN PRESCRIPTION DRUG Tamoxifen Citrate Tamoxifen Citrate TABLET, FILM COATED ORAL 20210827 N/A ANDA ANDA075797 Mayne Pharma Commercial LLC TAMOXIFEN CITRATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (51862-642-10)
51862-643-30 51862-643 HUMAN PRESCRIPTION DRUG Tamoxifen Citrate Tamoxifen Citrate TABLET, FILM COATED ORAL 20210827 N/A ANDA ANDA075797 Mayne Pharma Commercial LLC TAMOXIFEN CITRATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (51862-643-30)
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