80425-0102-2 |
80425-0102 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20101231 |
N/A |
ANDA |
ANDA090066 |
Advanced Rx Pharmacy 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 Pharmacy of Tennessee, LLC |
DICLOFENAC SODIUM |
50 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-3) |
35356-725-60 |
35356-725 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20130207 |
N/A |
ANDA |
ANDA090066 |
Quality Care Products LLC |
DICLOFENAC SODIUM |
50 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-725-60) |
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) |
68001-279-00 |
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) |
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) |
76420-571-01 |
76420-571 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA090066 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
25 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-01) |
76420-571-30 |
76420-571 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA090066 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
25 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-30) |
76420-571-60 |
76420-571 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA090066 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
25 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-60) |
76420-571-90 |
76420-571 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA090066 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
25 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-90) |
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) |