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 POTASSIUM | 50742-279-01 | Ingenus Pharmaceuticals, LLC | ANDA215585 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51021-250-05 | Sircle Laboratories, LLC | ANDA204132 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51316-012-15 | CVS PHARMACY, INC | ANDA208077 | HUMAN OTC DRUG | ANDA |
DICLOFENAC SODIUM | 51316-073-76 | CVS PHARMACY, INC | ANDA208077 | HUMAN OTC DRUG | ANDA |
DICLOFENAC POTASSIUM | 51407-443-01 | Golden State Medical Supply, Inc. | ANDA076561 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51655-176-26 | NORTHWIND PHARMACEUTICALS | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51655-176-52 | NORTHWIND PHARMACEUTICALS | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51655-176-84 | NORTHWIND PHARMACEUTICALS | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 51655-230-52 | Northwind Pharmaceuticals, LLC | ANDA075229 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51655-280-26 | Northwind Pharmaceuticals, LLC | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51655-280-52 | Northwind Pharmaceuticals, LLC | ANDA075185 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51655-308-52 | Northwind Pharmaceuticals | ANDA074514 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1358-2 | Taro Pharmaceuticals U.S.A., Inc. | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1358-4 | Taro Pharmaceuticals U.S.A., Inc. | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1363-3 | Taro Pharmaceuticals U.S.A., Inc. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1363-7 | Taro Pharmaceuticals U.S.A., Inc. | ANDA206298 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1369-8 | Taro Pharmaceuticals U.S.A., Inc. | ANDA208098 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52565-002-05 | Teligent Pharma, Inc. | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52565-002-59 | Teligent Pharma, Inc. | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-02 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-10 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-14 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-15 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-20 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-21 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-28 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-30 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-60 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52959-423-90 | H.J. Harkins Company Inc. dba Pharma Pac | ANDA077863 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC EPOLAMINE | 52959-518-05 | H.J. Harkins Company Inc. dba Pharma Pac | NDA021234 | HUMAN PRESCRIPTION DRUG | NDA |
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