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"
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
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)
63187-714-15 63187-714 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20160601 N/A ANDA ANDA090066 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 15 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-15)
63187-714-30 63187-714 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20160601 N/A ANDA ANDA090066 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-30)
63187-714-60 63187-714 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20160601 N/A ANDA ANDA090066 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-60)
63187-714-90 63187-714 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20160601 N/A ANDA ANDA090066 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-90)
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)
68788-8784-8 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/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-8)
68788-8784-9 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 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-9)
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)
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)
50090-0540-0 50090-0540 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20141128 N/A ANDA ANDA090066 A-S Medication Solutions DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0540-0)
50090-0540-2 50090-0540 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20141128 N/A ANDA ANDA090066 A-S Medication Solutions DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0540-2)
50090-0540-5 50090-0540 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220328 N/A ANDA ANDA090066 A-S Medication Solutions DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0540-5)
16571-203-03 16571-203 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240722 N/A ANDA ANDA090066 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 25 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-203-03)
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