FDA Application
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NDC Search Results on Active Ingredient: Diclofenac
Click on Active Ingredient to view the label.
| Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| DICLOFENAC SODIUM | 58602-604-22 | Aurohealth LLC | ANDA204306 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 58602-604-23 | Aurohealth LLC | ANDA204306 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 58602-606-21 | Aurohealth LLC | ANDA204306 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 58602-609-07 | Aurohealth LLC | ANDA204306 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM; CAPSICUM OLEORESIN | 59088-093-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| DICLOFENAC SODIUM | 59088-372-10 | PureTek Corporation | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 59088-435-10 | PureTek Corporation | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 59088-709-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| DICLOFENAC SODIUM | 59088-727-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| DICLOFENAC SODIUM; CAPSICUM OLEORESIN | 59088-801-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| DICLOFENAC SODIUM | 59390-149-02 | Altaire Pharmaceuticals Inc. | ANDA203383 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 59390-149-05 | Altaire Pharmaceuticals Inc. | ANDA203383 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 59651-353-01 | Aurobindo Pharma Limited | ANDA213875 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 59651-353-08 | Aurobindo Pharma Limited | ANDA213875 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 59726-012-50 | P & L Development, LLC | ANDA208077 | HUMAN OTC DRUG | ANDA |
| DICLOFENAC SODIUM | 59726-012-53 | P & L Development, LLC | ANDA208077 | HUMAN OTC DRUG | ANDA |
| MISOPROSTOL; DICLOFENAC SODIUM | 59762-0028-1 | Greenstone LLC | NDA020607 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| MISOPROSTOL; DICLOFENAC SODIUM | 59762-0028-2 | Greenstone LLC | NDA020607 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| DICLOFENAC SODIUM; MISOPROSTOL | 59762-0029-1 | Greenstone LLC | NDA020607 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| DICLOFENAC EPOLAMINE | 59762-0707-1 | Greenstone LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC EPOLAMINE | 59762-0707-2 | Greenstone LLC | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| DICLOFENAC POTASSIUM | 60290-057-01 | UMEDICA LABORATORIES PRIVATE LIMITED | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 60290-057-02 | UMEDICA LABORATORIES PRIVATE LIMITED | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC POTASSIUM | 60290-057-03 | UMEDICA LABORATORIES PRIVATE LIMITED | ANDA215750 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 60429-421-01 | Golden State Medical Supply, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 60429-421-10 | Golden State Medical Supply, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 60429-421-18 | Golden State Medical Supply, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 60429-422-01 | Golden State Medical Supply, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 60429-422-10 | Golden State Medical Supply, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
| DICLOFENAC SODIUM | 60429-422-18 | Golden State Medical Supply, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
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