| 71335-0481-1 |
71335-0481 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180515 |
N/A |
ANDA |
ANDA075185 |
Bryant Ranch Prepack |
DICLOFENAC SODIUM |
50 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-1) |
| 71335-0481-2 |
71335-0481 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180221 |
N/A |
ANDA |
ANDA075185 |
Bryant Ranch Prepack |
DICLOFENAC SODIUM |
50 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-2) |
| 71335-0481-3 |
71335-0481 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180228 |
N/A |
ANDA |
ANDA075185 |
Bryant Ranch Prepack |
DICLOFENAC SODIUM |
50 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-3) |
| 63629-2012-1 |
63629-2012 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
19981113 |
N/A |
ANDA |
ANDA075185 |
Bryant Ranch Prepack |
DICLOFENAC SODIUM |
75 mg/1 |
12 BOTTLE, PLASTIC in 1 BOX (63629-2012-1) / 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
| 68788-9806-1 |
68788-9806 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20150831 |
N/A |
ANDA |
ANDA075185 |
Preferred Pharmaceuticals Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-9806-1) |
| 68788-9806-2 |
68788-9806 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20150831 |
N/A |
ANDA |
ANDA075185 |
Preferred Pharmaceuticals Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68788-9806-2) |
| 70518-0756-0 |
70518-0756 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20171004 |
N/A |
ANDA |
ANDA075185 |
REMEDYREPACK INC. |
DICLOFENAC SODIUM |
50 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0756-0) |
| 63629-2013-1 |
63629-2013 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
19981113 |
N/A |
ANDA |
ANDA075185 |
Bryant Ranch Prepack |
DICLOFENAC SODIUM |
75 mg/1 |
24 BOTTLE, PLASTIC in 1 BOX (63629-2013-1) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
| 68071-3184-1 |
68071-3184 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170321 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals, Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
21 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-1) |
| 68071-3184-2 |
68071-3184 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170321 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals, Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
20 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-2) |
| 68071-3184-3 |
68071-3184 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170321 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals, Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-3) |
| 68071-3184-5 |
68071-3184 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170321 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals, Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
45 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-5) |
| 68071-3184-6 |
68071-3184 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170321 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals, Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-6) |
| 68071-3184-9 |
68071-3184 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170321 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals, Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-9) |
| 68071-4117-2 |
68071-4117 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20171011 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
20 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-2) |
| 68071-4117-3 |
68071-4117 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20171011 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-3) |
| 68071-4117-4 |
68071-4117 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20171011 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-4) |
| 68071-4117-6 |
68071-4117 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20171011 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-6) |
| 68071-4117-9 |
68071-4117 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20171011 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4117-9) |
| 71205-995-00 |
71205-995 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20200401 |
N/A |
ANDA |
ANDA075185 |
Proficient Rx LP |
DICLOFENAC SODIUM |
50 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-00) |