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=ANDA090066"
符合检索条件的记录共 42 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
71335-2543-5 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-5)
71335-2543-6 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-6)
71335-2543-7 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-7)
68001-279-00 68001-279 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 25 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-279-00)
76420-572-01 76420-572 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA090066 Asclemed USA, Inc. DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-01)
76420-572-30 76420-572 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA090066 Asclemed USA, Inc. DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-30)
76420-572-60 76420-572 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA090066 Asclemed USA, Inc. DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-60)
76420-572-90 76420-572 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA090066 Asclemed USA, Inc. DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-90)
60687-606-01 60687-606 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220607 N/A ANDA ANDA090066 American Health Packaging DICLOFENAC SODIUM 50 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-606-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-606-11)
68001-280-00 68001-280 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-00)
68001-280-06 68001-280 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-06)
68001-280-08 68001-280 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 50 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-08)
16571-202-06 16571-202 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20101231 N/A ANDA ANDA090066 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-202-06)
16571-202-10 16571-202 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20101231 N/A ANDA ANDA090066 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-202-10)
16571-202-11 16571-202 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20101231 N/A ANDA ANDA090066 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 50 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-202-11)
80425-0102-2 80425-0102 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20101231 N/A ANDA ANDA090066 Advanced Rx of Tennessee, LLC DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-2)
80425-0102-3 80425-0102 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20101231 N/A ANDA ANDA090066 Advanced Rx of Tennessee, LLC DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-3)
68788-8784-1 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-1)
68788-8784-3 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-3)
68788-8784-6 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-6)
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