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 EPOLAMINE | 52959-518-30 | H.J. Harkins Company Inc. dba Pharma Pac | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA |
DICLOFENAC POTASSIUM | 52959-659-20 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 52959-659-28 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 52959-659-30 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 52959-659-40 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 52959-659-60 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 52959-659-90 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-987-05 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA078792 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 53002-1176-3 | RPK Pharmaceuticals, Inc. | ANDA075219 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-1792-1 | RPK Pharmaceuticals, Inc. | ANDA075492 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-1792-2 | RPK Pharmaceuticals, Inc. | ANDA075492 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-1792-3 | RPK Pharmaceuticals, Inc. | ANDA075492 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-3325-2 | RPK Pharmaceuticals, Inc. | ANDA078792 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-4642-1 | RPK Pharmaceuticals, Inc. | ANDA210986 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-5360-1 | RPK Pharmaceuticals, Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-5360-2 | RPK Pharmaceuticals, Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-5360-3 | RPK Pharmaceuticals, Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-5360-5 | RPK Pharmaceuticals, Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53002-5370-3 | RPK Pharmaceuticals, Inc. | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53149-4901-1 | All Pharma, LLC | ANDA208301 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53149-4902-1 | All Pharma, LLC | ANDA206116 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 53217-099-01 | Aidarex Pharmaceuticals LLC | ANDA078031 | HUMAN PRESCRIPTION DRUG | ANDA |
LIDOCAINE; DICLOFENAC SODIUM | 53225-1070-1 | Terrain Pharmaceuticals | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
LIDOCAINE HYDROCHLORIDE; DICLOFENAC SODIUM | 53225-1076-1 | Terrain Pharmaceuticals | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 53943-523-01 | Discount Drug Mart, Inc. | ANDA210986 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 55289-150-10 | PD-Rx Pharmaceuticals, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 55289-150-15 | PD-Rx Pharmaceuticals, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 55289-150-20 | PD-Rx Pharmaceuticals, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 55289-150-28 | PD-Rx Pharmaceuticals, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 55289-150-30 | PD-Rx Pharmaceuticals, Inc. | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
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