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=ANDA075576"
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
71335-0332-1 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20180716 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-1)
71335-0332-2 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20200325 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-2)
71335-0332-3 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240528 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 56 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-3)
71335-0332-4 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20200508 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-4)
71335-0332-5 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20200603 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-5)
71335-0332-6 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20180706 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 15 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-6)
71335-0332-7 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20200312 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-7)
71335-0332-8 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240528 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-8)
71335-0332-9 71335-0332 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240528 N/A ANDA ANDA075576 Bryant Ranch Prepack OMEPRAZOLE 20 mg/1 28 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-0332-9)
60760-833-30 60760-833 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20240730 N/A ANDA ANDA075576 ST. MARY'S MEDICAL PARK PHARMACY OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-833-30)
43063-743-14 43063-743 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170324 N/A ANDA ANDA075576 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-743-14)
43063-743-30 43063-743 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170208 N/A ANDA ANDA075576 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-743-30)
43063-743-60 43063-743 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170324 N/A ANDA ANDA075576 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-743-60)
43063-743-90 43063-743 HUMAN PRESCRIPTION DRUG Omeprazole Omeprazole CAPSULE, DELAYED RELEASE ORAL 20170324 N/A ANDA ANDA075576 PD-Rx Pharmaceuticals, Inc. OMEPRAZOLE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (43063-743-90)
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