Diclofenac Potassium is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by H.j. Harkins Company, Inc.. The primary component is Diclofenac Potassium.
| Product ID | 52959-659_a346079a-144b-47b0-ba63-cd3db2c05ce2 |
| NDC | 52959-659 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Diclofenac Potassium |
| Generic Name | Diclofenac Potassium |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-01-21 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA075219 |
| Labeler Name | H.J. Harkins Company, Inc. |
| Substance Name | DICLOFENAC POTASSIUM |
| Active Ingredient Strength | 50 mg/1 |
| Pharm Classes | Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2010-01-21 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA075219 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-21 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA075219 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-21 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA075219 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-21 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA075219 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-21 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA075219 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-21 |
| Inactivation Date | 2019-11-13 |
| Marketing Category | ANDA |
| Application Number | ANDA075219 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-01-21 |
| Inactivation Date | 2019-11-13 |
| Ingredient | Strength |
|---|---|
| DICLOFENAC POTASSIUM | 50 mg/1 |
| SPL SET ID: | 0c3ac260-586d-4203-855b-f7518e89484e |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0093-0948 | Diclofenac Potassium | Diclofenac Potassium |
| 0378-2474 | Diclofenac Potassium | diclofenac potassium |
| 0480-9435 | Diclofenac potassium | diclofenac potassium |
| 0781-5017 | Diclofenac Potassium | Diclofenac Potassium |
| 12634-827 | DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM |
| 21695-838 | Diclofenac Potassium | Diclofenac Potassium |
| 23155-840 | diclofenac potassium | diclofenac potassium |
| 31722-046 | Diclofenac potassium | Diclofenac potassium |
| 33261-038 | Diclofenac Potassium | Diclofenac Potassium |
| 35356-713 | Diclofenac Potassium | Diclofenac Potassium |
| 43063-848 | Diclofenac Potassium | Diclofenac Potassium |
| 49884-905 | Diclofenac Potassium | Diclofenac Potassium |
| 50090-0646 | Diclofenac Potassium | Diclofenac Potassium |
| 50090-0647 | Diclofenac Potassium | Diclofenac Potassium |
| 50090-1535 | Diclofenac Potassium | diclofenac potassium |
| 50090-5893 | Diclofenac Potassium | diclofenac potassium |
| 68071-4042 | Diclofenac Potassium | Diclofenac Potassium |
| 68151-0561 | Diclofenac Potassium | Diclofenac Potassium |
| 71335-0369 | Diclofenac Potassium | Diclofenac Potassium |
| 52959-659 | Diclofenac Potassium | Diclofenac Potassium |
| 53002-1176 | Diclofenac Potassium | Diclofenac Potassium |
| 55289-781 | Diclofenac Potassium | Diclofenac Potassium |
| 61919-072 | DICLOFENAC POTASSIUM | DICLOFENAC POTASSIUM |
| 63629-4108 | Diclofenac Potassium | Diclofenac Potassium |
| 66267-070 | Diclofenac Potassium | Diclofenac Potassium |
| 67296-1316 | Diclofenac Potassium | Diclofenac Potassium |
| 63629-7969 | Diclofenac Potassium | Diclofenac Potassium |
| 70518-2185 | Diclofenac Potassium | Diclofenac Potassium |
| 67296-1746 | Diclofenac Potassium | Diclofenac Potassium |
| 72789-051 | Diclofenac Potassium | Diclofenac Potassium |
| 69292-550 | Diclofenac Potassium | Diclofenac Potassium |
| 13913-011 | Cambia | diclofenac potassium |
| 13913-012 | Cambia | diclofenac potassium |
| 50192-113 | CAMBIA | Diclofenac Potassium |
| 15370-180 | LOFENA | DICLOFENAC POTASSIUM |
| 13913-008 | ZIPSOR | diclofenac potassium |