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=ANDA206582"
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
63548-2970-2 63548-2970 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20241031 N/A ANDA ANDA206582 PLD Acquisitions LLC DBA Avéma Pharma Solutions OMEPRAZOLE MAGNESIUM 20.6 mg/1 1 BOTTLE, PLASTIC in 1 BOX (63548-2970-2) / 42 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
63548-2970-4 63548-2970 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20241031 N/A ANDA ANDA206582 PLD Acquisitions LLC DBA Avéma Pharma Solutions OMEPRAZOLE MAGNESIUM 20.6 mg/1 1 BOTTLE, PLASTIC in 1 BOX (63548-2970-4) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
63548-2970-8 63548-2970 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20241031 N/A ANDA ANDA206582 PLD Acquisitions LLC DBA Avéma Pharma Solutions OMEPRAZOLE MAGNESIUM 20.6 mg/1 1 BOTTLE, PLASTIC in 1 BOX (63548-2970-8) / 28 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
59726-744-42 59726-744 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20250829 N/A ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20 mg/1 3 BOTTLE, PLASTIC in 1 BOX (59726-744-42) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
59726-298-14 59726-298 HUMAN OTC DRUG Omeprazole Omeprazole TABLET, DELAYED RELEASE ORAL 20250131 N/A ANDA ANDA206582 P & L Development, LLC OMEPRAZOLE MAGNESIUM 20.6 mg/1 1 BOTTLE, PLASTIC in 1 BOX (59726-298-14) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
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