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=ANDA078777"
符合检索条件的记录共 46 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
70518-4239-3 70518-4239 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA078777 REMEDYREPACK INC. ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4239-3)
70518-4300-0 70518-4300 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20250303 N/A ANDA ANDA078777 REMEDYREPACK INC. ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4300-0)
70518-4300-1 70518-4300 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA078777 REMEDYREPACK INC. ESCITALOPRAM OXALATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4300-1)
71335-2460-1 71335-2460 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20240927 N/A ANDA ANDA078777 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2460-1)
71335-2460-2 71335-2460 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20241212 N/A ANDA ANDA078777 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2460-2)
71335-2460-3 71335-2460 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20240729 N/A ANDA ANDA078777 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2460-3)
71335-2460-4 71335-2460 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20241212 N/A ANDA ANDA078777 Bryant Ranch Prepack ESCITALOPRAM OXALATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2460-4)
16571-756-10 16571-756 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20230610 N/A ANDA ANDA078777 Rising Pharma Holdings, Inc. ESCITALOPRAM OXALATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-756-10)
16571-757-01 16571-757 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20230610 N/A ANDA ANDA078777 Rising Pharma Holdings, Inc. ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16571-757-01)
16571-757-10 16571-757 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20230610 N/A ANDA ANDA078777 Rising Pharma Holdings, Inc. ESCITALOPRAM OXALATE 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-757-10)
68788-8569-1 68788-8569 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20250408 N/A ANDA ANDA078777 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8569-1)
68788-8569-3 68788-8569 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20240123 N/A ANDA ANDA078777 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8569-3)
68788-8569-6 68788-8569 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20250408 N/A ANDA ANDA078777 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8569-6)
68788-8569-9 68788-8569 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20250408 N/A ANDA ANDA078777 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8569-9)
16571-756-01 16571-756 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20230610 N/A ANDA ANDA078777 Rising Pharma Holdings, Inc. ESCITALOPRAM OXALATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16571-756-01)
16571-755-10 16571-755 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20230610 N/A ANDA ANDA078777 Rising Pharma Holdings, Inc. ESCITALOPRAM OXALATE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16571-755-10)
16571-755-01 16571-755 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20230610 N/A ANDA ANDA078777 Rising Pharma Holdings, Inc. ESCITALOPRAM OXALATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16571-755-01)
68788-8723-1 68788-8723 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20240815 N/A ANDA ANDA078777 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8723-1)
68788-8723-9 68788-8723 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20240815 N/A ANDA ANDA078777 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8723-9)
68788-8723-3 68788-8723 HUMAN PRESCRIPTION DRUG escitalopram escitalopram TABLET, FILM COATED ORAL 20240815 N/A ANDA ANDA078777 Preferred Pharmaceuticals Inc. ESCITALOPRAM OXALATE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8723-3)
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