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=ANDA075410"
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
62135-530-30 62135-530 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20230316 N/A ANDA ANDA075410 Chartwell RX, LLC OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62135-530-30)
62135-530-90 62135-530 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20230316 N/A ANDA ANDA075410 Chartwell RX, LLC OMEPRAZOLE 10 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62135-530-90)
62175-114-32 62175-114 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20030903 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 10 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-32)
62175-114-37 62175-114 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20030903 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 10 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-37)
62175-114-46 62175-114 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20030903 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 10 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-114-46)
62175-114-49 62175-114 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20030903 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 10 mg/1 72000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-114-49)
62175-118-32 62175-118 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20021104 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-32)
62175-118-37 62175-118 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20021104 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-37)
62175-118-43 62175-118 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20021104 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-43)
62175-118-46 62175-118 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20021104 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-118-46)
62175-118-49 62175-118 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20021104 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 20 mg/1 54000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-118-49)
62175-136-32 62175-136 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20090123 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-32)
62175-136-37 62175-136 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20090123 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-37)
62175-136-43 62175-136 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20090123 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 40 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-43)
62175-136-46 62175-136 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20090123 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62175-136-46)
62175-136-49 62175-136 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20090123 N/A ANDA ANDA075410 Lannett Company, Inc. OMEPRAZOLE 40 mg/1 36000 CAPSULE, DELAYED RELEASE in 1 DRUM (62175-136-49)
53002-2688-0 53002-2688 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA075410 RPK Pharmaceuticals, Inc. OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53002-2688-0)
53002-2688-3 53002-2688 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20190101 N/A ANDA ANDA075410 RPK Pharmaceuticals, Inc. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53002-2688-3)
72789-155-90 72789-155 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20210112 N/A ANDA ANDA075410 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 40 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-155-90)
70518-2235-0 70518-2235 HUMAN PRESCRIPTION DRUG Omeprazole omeprazole CAPSULE, DELAYED RELEASE ORAL 20190725 N/A ANDA ANDA075410 REMEDYREPACK INC. OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-2235-0)
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