| 76420-393-01 |
76420-393 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250618 |
N/A |
ANDA |
ANDA077863 |
ASCLEMED USA INC. |
DICLOFENAC SODIUM |
75 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-393-01) |
| 76420-393-14 |
76420-393 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250924 |
N/A |
ANDA |
ANDA077863 |
ASCLEMED USA INC. |
DICLOFENAC SODIUM |
75 mg/1 |
14 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-393-14) |
| 76420-393-30 |
76420-393 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250618 |
N/A |
ANDA |
ANDA077863 |
ASCLEMED USA INC. |
DICLOFENAC SODIUM |
75 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-393-30) |
| 76420-393-60 |
76420-393 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250618 |
N/A |
ANDA |
ANDA077863 |
ASCLEMED USA INC. |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-393-60) |
| 76420-393-90 |
76420-393 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250618 |
N/A |
ANDA |
ANDA077863 |
ASCLEMED USA INC. |
DICLOFENAC SODIUM |
75 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-393-90) |
| 50090-6924-0 |
50090-6924 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20231214 |
N/A |
ANDA |
ANDA077863 |
A-S Medication Solutions |
DICLOFENAC SODIUM |
75 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6924-0) |
| 68001-281-00 |
68001-281 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20151221 |
N/A |
ANDA |
ANDA077863 |
BluePoint Laboratories |
DICLOFENAC SODIUM |
75 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-00) |
| 68001-281-03 |
68001-281 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20151221 |
N/A |
ANDA |
ANDA077863 |
BluePoint Laboratories |
DICLOFENAC SODIUM |
75 mg/1 |
500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-03) |
| 68001-281-06 |
68001-281 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20151221 |
N/A |
ANDA |
ANDA077863 |
BluePoint Laboratories |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-281-06) |
| 68001-281-08 |
68001-281 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20151221 |
N/A |
ANDA |
ANDA077863 |
BluePoint Laboratories |
DICLOFENAC SODIUM |
75 mg/1 |
1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-08) |
| 76420-670-01 |
76420-670 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA077863 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-01) |
| 76420-670-30 |
76420-670 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA077863 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-30) |
| 76420-670-60 |
76420-670 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA077863 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-60) |
| 76420-670-90 |
76420-670 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20240307 |
N/A |
ANDA |
ANDA077863 |
Asclemed USA, Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-90) |
| 80425-0056-1 |
80425-0056 |
HUMAN PRESCRIPTION DRUG |
Diclofenac DR |
Diclofenac |
TABLET, DELAYED RELEASE |
ORAL |
20080819 |
N/A |
ANDA |
ANDA077863 |
Advanced Rx of Tennessee, LLC |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0056-1) |
| 67046-1482-3 |
67046-1482 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250129 |
N/A |
ANDA |
ANDA077863 |
Coupler LLC |
DICLOFENAC SODIUM |
75 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-1482-3) |
| 85509-1201-3 |
85509-1201 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20260107 |
N/A |
ANDA |
ANDA077863 |
PHOENIX RX LLC |
DICLOFENAC SODIUM |
75 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-3) |
| 85509-1201-6 |
85509-1201 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20260107 |
N/A |
ANDA |
ANDA077863 |
PHOENIX RX LLC |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1201-6) |
| 85509-1201-9 |
85509-1201 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20260107 |
N/A |
ANDA |
ANDA077863 |
PHOENIX RX LLC |
DICLOFENAC SODIUM |
75 mg/1 |
90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-9) |
| 68788-8193-1 |
68788-8193 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20220516 |
N/A |
ANDA |
ANDA077863 |
Preferred Pharmaceuticals Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8193-1) |