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=ANDA078216"
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
55700-851-90 55700-851 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20200820 20261031 ANDA ANDA078216 Quality Care Products, LLC CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET in 1 BOTTLE (55700-851-90)
50090-6846-0 50090-6846 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20231129 N/A ANDA ANDA078216 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 20 mg/1 90 TABLET in 1 BOTTLE (50090-6846-0)
0904-6085-61 0904-6085 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20091102 N/A ANDA ANDA078216 Major Pharmaceuticals CITALOPRAM HYDROBROMIDE 20 mg/1 100 BLISTER PACK in 1 CARTON (0904-6085-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
13668-010-01 13668-010 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20071018 N/A ANDA ANDA078216 Torrent Pharmaceuticals Limited CITALOPRAM HYDROBROMIDE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (13668-010-01)
13668-010-05 13668-010 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20071018 N/A ANDA ANDA078216 Torrent Pharmaceuticals Limited CITALOPRAM HYDROBROMIDE 20 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (13668-010-05)
13668-010-06 13668-010 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20071018 N/A ANDA ANDA078216 Torrent Pharmaceuticals Limited CITALOPRAM HYDROBROMIDE 20 mg/1 5600 TABLET, FILM COATED in 1 BOTTLE (13668-010-06)
13668-010-30 13668-010 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20071018 N/A ANDA ANDA078216 Torrent Pharmaceuticals Limited CITALOPRAM HYDROBROMIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (13668-010-30)
50090-3208-0 50090-3208 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20171024 N/A ANDA ANDA078216 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET in 1 BOTTLE (50090-3208-0)
68788-8962-6 68788-8962 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160104 N/A ANDA ANDA078216 Preferred Pharmaceuticals Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8962-6)
70518-4476-0 70518-4476 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20250911 N/A ANDA ANDA078216 REMEDYREPACK INC. CITALOPRAM HYDROBROMIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4476-0)
70518-4476-1 70518-4476 HUMAN PRESCRIPTION DRUG Citalopram Citalopram TABLET, FILM COATED ORAL 20260122 N/A ANDA ANDA078216 REMEDYREPACK INC. CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4476-1)
71205-764-30 71205-764 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20230214 N/A ANDA ANDA078216 Proficient Rx LP CITALOPRAM HYDROBROMIDE 40 mg/1 30 TABLET in 1 BOTTLE (71205-764-30)
71205-764-60 71205-764 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20230214 N/A ANDA ANDA078216 Proficient Rx LP CITALOPRAM HYDROBROMIDE 40 mg/1 60 TABLET in 1 BOTTLE (71205-764-60)
71205-764-90 71205-764 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20230214 N/A ANDA ANDA078216 Proficient Rx LP CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET in 1 BOTTLE (71205-764-90)
68788-8962-8 68788-8962 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160104 N/A ANDA ANDA078216 Preferred Pharmaceuticals Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 120 TABLET, FILM COATED in 1 CARTON (68788-8962-8)
68788-8962-9 68788-8962 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20160104 N/A ANDA ANDA078216 Preferred Pharmaceuticals Inc. CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8962-9)
51655-043-26 51655-043 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20250422 N/A ANDA ANDA078216 Northwind Health Company, LLC CITALOPRAM HYDROBROMIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-043-26)
51655-043-52 51655-043 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET, FILM COATED ORAL 20210324 N/A ANDA ANDA078216 Northwind Health Company, LLC CITALOPRAM HYDROBROMIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-043-52)
50090-3208-1 50090-3208 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20171026 N/A ANDA ANDA078216 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 40 mg/1 100 TABLET in 1 BOTTLE (50090-3208-1)
50090-3208-2 50090-3208 HUMAN PRESCRIPTION DRUG Citalopram Hydrobromide Citalopram Hydrobromide TABLET ORAL 20171024 N/A ANDA ANDA078216 A-S Medication Solutions CITALOPRAM HYDROBROMIDE 40 mg/1 90 TABLET in 1 BOTTLE (50090-3208-2)
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