| 50090-7880-1 |
50090-7880 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20260204 |
N/A |
ANDA |
ANDA075185 |
A-S Medication Solutions |
DICLOFENAC SODIUM |
50 mg/1 |
14 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7880-1) |
| 63629-2077-1 |
63629-2077 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20210204 |
N/A |
ANDA |
ANDA075185 |
Bryant Ranch Prepack |
DICLOFENAC SODIUM |
50 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-2077-1) |
| 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) |
| 68071-4231-1 |
68071-4231 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180112 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
21 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4231-1) |
| 68071-4231-3 |
68071-4231 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180112 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4231-3) |
| 68071-4231-5 |
68071-4231 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180112 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
45 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4231-5) |
| 68071-4231-6 |
68071-4231 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180112 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4231-6) |
| 68071-4231-9 |
68071-4231 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180112 |
N/A |
ANDA |
ANDA075185 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
50 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4231-9) |
| 71205-494-30 |
71205-494 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20201020 |
N/A |
ANDA |
ANDA075185 |
Proficient Rx LP |
DICLOFENAC SODIUM |
50 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-494-30) |
| 71205-494-60 |
71205-494 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20201020 |
N/A |
ANDA |
ANDA075185 |
Proficient Rx LP |
DICLOFENAC SODIUM |
50 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-494-60) |
| 71205-494-90 |
71205-494 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20201020 |
N/A |
ANDA |
ANDA075185 |
Proficient Rx LP |
DICLOFENAC SODIUM |
50 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-494-90) |
| 61145-101-06 |
61145-101 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170927 |
N/A |
ANDA |
ANDA075185 |
REPHARM LLC |
DICLOFENAC SODIUM |
50 mg/1 |
24 BOTTLE, PLASTIC in 1 BOX (61145-101-06) / 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
| 61145-101-09 |
61145-101 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170927 |
N/A |
ANDA |
ANDA075185 |
REPHARM LLC |
DICLOFENAC SODIUM |
50 mg/1 |
24 BOTTLE, PLASTIC in 1 BOX (61145-101-09) / 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
| 61145-101-18 |
61145-101 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20170927 |
N/A |
ANDA |
ANDA075185 |
REPHARM LLC |
DICLOFENAC SODIUM |
50 mg/1 |
24 BOTTLE, PLASTIC in 1 BOX (61145-101-18) / 180 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC |
| 70518-0627-1 |
70518-0627 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium Delayed Release |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20171023 |
N/A |
ANDA |
ANDA075185 |
REMEDYREPACK INC. |
DICLOFENAC SODIUM |
75 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0627-1) |