Drugs@FDA: FDA-Approved Drugs
Company: RUBICON RESEARCH
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | TE Code | RLD | RS |
|---|---|---|---|---|---|---|---|
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | AB | No | Yes |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 25MG | TABLET;ORAL | Prescription | AB | No | No |
Original Approvals or Tentative Approvals
| Action Date | Submission | Action Type | Submission Classification | Review Priority; Orphan Status | Letters, Reviews, Labels, Patient Package Insert | Notes | Url |
|---|---|---|---|---|---|---|---|
| 11/20/1998 | ORIG-1 | Approval |
Letter (PDF)
|
Label is not available on this site. |
https://www.accessdata.fda.gov/drugsatfda_docs/appletter/1998/75229ltr.pdf |
Supplements
| Action Date | Submission | Supplement Categories or Approval Type | Letters, Reviews, Labels, Patient Package Insert | Note | Url |
|---|---|---|---|---|---|
| 11/21/2024 | SUPPL-35 | Labeling-Package Insert |
Label is not available on this site. |
||
| 04/28/2021 | SUPPL-23 | Labeling-Package Insert |
Label is not available on this site. |
||
| 04/26/2021 | SUPPL-20 | Labeling-Package Insert |
Label is not available on this site. |
||
| 12/06/2014 | SUPPL-16 | Labeling-Package Insert |
Label is not available on this site. |
||
| 09/04/2009 | SUPPL-14 | Labeling-Package Insert |
Label is not available on this site. |
||
| 04/29/2008 | SUPPL-12 | Labeling |
Label is not available on this site. |
||
| 10/05/2006 | SUPPL-11 | Labeling |
Label is not available on this site. |
||
| 09/10/2002 | SUPPL-6 | Labeling |
Label is not available on this site. |
||
| 10/02/2002 | SUPPL-5 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
||
| 10/02/2002 | SUPPL-4 | Manufacturing (CMC)-Control |
Label is not available on this site. |
||
| 10/02/2002 | SUPPL-3 | Manufacturing (CMC)-Facility |
Label is not available on this site. |
||
| 03/18/2002 | SUPPL-2 | Manufacturing (CMC)-Facility |
Label is not available on this site. |
||
| 03/18/2002 | SUPPL-1 | Manufacturing (CMC)-Packaging |
Label is not available on this site. |
DICLOFENAC POTASSIUM
TABLET;ORAL; 50MG
TE Code = AB
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
|---|---|---|---|---|---|---|---|---|
| CATAFLAM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | No | AB | 076561 | AMICI PHARMA |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | No | AB | 215585 | INGENUS PHARMS LLC |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | No | AB | 075463 | RK PHARMA |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | No | AB | 075229 | RUBICON RESEARCH |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | No | AB | 215787 | SENORES PHARMS |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | No | AB | 075219 | TEVA |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 50MG | TABLET;ORAL | Prescription | No | AB | 215750 | UMEDICA |
TABLET;ORAL; 25MG
TE Code = AB
| Drug Name | Active Ingredients | Strength | Dosage Form/Route | Marketing Status | RLD | TE Code | Application No. | Company |
|---|---|---|---|---|---|---|---|---|
| CATAFLAM | DICLOFENAC POTASSIUM | 25MG | TABLET;ORAL | Prescription | No | AB | 076561 | AMICI PHARMA |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 25MG | TABLET;ORAL | Prescription | No | AB | 075229 | RUBICON RESEARCH |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 25MG | TABLET;ORAL | Prescription | No | AB | 215787 | SENORES PHARMS |
| DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM | 25MG | TABLET;ORAL | Prescription | No | AB | 215750 | UMEDICA |