| 66267-071-14 |
66267-071 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180116 |
N/A |
ANDA |
ANDA077863 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
14 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-071-14) |
| 66267-071-20 |
66267-071 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20180116 |
N/A |
ANDA |
ANDA077863 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
20 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-071-20) |
| 66267-071-60 |
66267-071 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20250114 |
N/A |
ANDA |
ANDA077863 |
NuCare Pharmaceuticals,Inc. |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-071-60) |
| 63187-012-15 |
63187-012 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20191122 |
N/A |
ANDA |
ANDA077863 |
Proficient Rx LP |
DICLOFENAC SODIUM |
75 mg/1 |
15 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-15) |
| 63187-012-20 |
63187-012 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20161101 |
N/A |
ANDA |
ANDA077863 |
Proficient Rx LP |
DICLOFENAC SODIUM |
75 mg/1 |
20 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-20) |
| 63187-012-30 |
63187-012 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20140401 |
N/A |
ANDA |
ANDA077863 |
Proficient Rx LP |
DICLOFENAC SODIUM |
75 mg/1 |
30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-30) |
| 63187-012-60 |
63187-012 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20141001 |
N/A |
ANDA |
ANDA077863 |
Proficient Rx LP |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-012-60) |
| 35356-714-60 |
35356-714 |
HUMAN PRESCRIPTION DRUG |
Diclofenac Sodium |
Diclofenac Sodium |
TABLET, DELAYED RELEASE |
ORAL |
20130207 |
20260731 |
ANDA |
ANDA077863 |
Quality Care Products LLC |
DICLOFENAC SODIUM |
75 mg/1 |
60 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-714-60) |
| 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) |
| 76420-670-60 |
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) |