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=ANDA078490"
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
50090-7472-7 50090-7472 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 20 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-7)
50090-7472-8 50090-7472 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA078490 A-S Medication Solutions OMEPRAZOLE 20 mg/1 7 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-7472-8)
60687-597-01 60687-597 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20251201 N/A ANDA ANDA078490 American Health Packaging OMEPRAZOLE 20 mg/1 100 BLISTER PACK in 1 CARTON (60687-597-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-597-11)
55111-644-01 55111-644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-01)
55111-644-05 55111-644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 20 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-05)
55111-644-10 55111-644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-10)
55111-644-30 55111-644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-644-30)
55111-644-77 55111-644 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20140301 N/A ANDA ANDA078490 Dr. Reddy's Laboratories Limited OMEPRAZOLE 20 mg/1 1 BLISTER PACK in 1 CARTON (55111-644-77) / 7 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
71610-912-53 71610-912 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250902 N/A ANDA ANDA078490 Aphena Pharma Solutions - Tennessee, LLC OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-912-53)
71610-912-60 71610-912 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250605 N/A ANDA ANDA078490 Aphena Pharma Solutions - Tennessee, LLC OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-912-60)
71610-912-80 71610-912 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250902 N/A ANDA ANDA078490 Aphena Pharma Solutions - Tennessee, LLC OMEPRAZOLE 20 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-912-80)
16714-123-01 16714-123 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20191025 N/A ANDA ANDA078490 NorthStar Rx LLC OMEPRAZOLE 40 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-123-01)
16714-123-02 16714-123 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20191025 N/A ANDA ANDA078490 NorthStar Rx LLC OMEPRAZOLE 40 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-123-02)
16714-123-03 16714-123 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20191025 N/A ANDA ANDA078490 NorthStar Rx LLC OMEPRAZOLE 40 mg/1 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16714-123-03)
68071-3733-6 68071-3733 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20250303 N/A ANDA ANDA078490 NuCare Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3733-6)
68071-3733-9 68071-3733 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20241202 N/A ANDA ANDA078490 NuCare Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3733-9)
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