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=ANDA075511"
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
43063-533-30 43063-533 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20140414 N/A ANDA ANDA075511 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-533-30)
50090-6932-0 50090-6932 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20231214 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6932-0)
0615-4582-05 0615-4582 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20100430 N/A ANDA ANDA075511 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 20 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-4582-05)
0615-4582-39 0615-4582 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20100430 N/A ANDA ANDA075511 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-4582-39)
0615-8301-05 0615-8301 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20230831 N/A ANDA ANDA075511 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 40 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8301-05)
0615-8301-39 0615-8301 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20190701 N/A ANDA ANDA075511 NCS HealthCare of KY, LLC dba Vangard Labs FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8301-39)
50090-1044-0 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-1044-0)
50090-1044-1 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-1044-1)
50090-1044-2 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-1044-2)
50090-1044-3 50090-1044 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20181005 N/A ANDA ANDA075511 A-S Medication Solutions FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-1044-3)
45865-881-51 45865-881 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20180601 N/A ANDA ANDA075511 Medsource Pharmaceuticals FAMOTIDINE 20 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (45865-881-51)
45865-881-60 45865-881 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20180601 N/A ANDA ANDA075511 Medsource Pharmaceuticals FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (45865-881-60)
68071-3181-2 68071-3181 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20180117 N/A ANDA ANDA075511 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3181-2)
68071-3181-3 68071-3181 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20180117 N/A ANDA ANDA075511 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3181-3)
68071-3181-6 68071-3181 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20180117 N/A ANDA ANDA075511 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-3181-6)
68071-3181-8 68071-3181 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20180117 N/A ANDA ANDA075511 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (68071-3181-8)
68071-3181-9 68071-3181 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20180117 N/A ANDA ANDA075511 NuCare Pharmaceuticals,Inc. FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3181-9)
68645-140-59 68645-140 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20091026 N/A ANDA ANDA075511 Legacy Pharmaceutical Packaging, LLC FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68645-140-59)
43063-086-06 43063-086 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20110211 N/A ANDA ANDA075511 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-086-06)
71205-276-10 71205-276 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA075511 Proficient Rx LP FAMOTIDINE 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71205-276-10)
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