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 |
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DICLOFENAC SODIUM | 72559-020-49 | Little Pharma, Inc. | ANDA210986 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 72578-092-01 | Viona Pharmaceuticals Inc | ANDA206411 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72819-151-10 | Archis Pharma LLC | ANDA075463 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM; MENTHOL; METHYL SALICYLATE | 72835-201-02 | V2 Pharma, LLC | ANDA202027 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM; METHYL SALICYLATE; MENTHOL | 72835-202-02 | V2 Pharma, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
LEFLUNOMIDE; DICLOFENAC SODIUM | 72835-602-02 | V2 Pharma, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
MENTHOL; CAMPHOR (SYNTHETIC); DICLOFENAC SODIUM | 72835-701-02 | V2 Pharma, LLC | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72888-073-00 | Advagen Pharma Ltd | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72888-073-01 | Advagen Pharma Ltd | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72888-073-05 | Advagen Pharma Ltd | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72888-073-30 | Advagen Pharma Ltd | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72888-086-00 | Advagen Pharma Ltd | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72888-086-01 | Advagen Pharma Ltd | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 72888-086-30 | Advagen Pharma Ltd | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-109-00 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-109-01 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-109-05 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-109-30 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-109-60 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-110-00 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-110-01 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-110-05 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-110-30 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-110-60 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-111-00 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-111-01 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-111-05 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-111-30 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72888-111-60 | Advagen Pharma Ltd | ANDA216548 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72934-1072-2 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other |
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