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 | 71205-450-15 | Proficient Rx LP | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM; MENTHOL | 72275-719-77 | Primary Pharmaceuticals, Inc | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 52565-002-05 | Teligent Pharma, Inc. | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 59088-372-10 | PureTek Corporation | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM; CAPSAICIN | 70859-058-01 | NuCare Pharmaceuticals,Inc. | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-2225-1 | Unit Dose Services | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
LIDOCAINE; METHYL SALICYLATE; CAMPHOR (NATURAL); DICLOFENAC SODIUM | 72275-702-77 | Primary Pharmaceuticals, Inc | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 60760-112-95 | St. Mary's Medical Park Pharmacy | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 55700-591-15 | Quality Care Products LLC | ANDA202769 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 49884-905-52 | Par Pharmaceutical, Inc. | ANDA202964 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 49884-905-24 | Par Pharmaceutical, Inc. | ANDA202964 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC POTASSIUM | 49884-905-64 | Par Pharmaceutical, Inc. | ANDA202964 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 59390-149-05 | Altaire Pharmaceuticals Inc. | ANDA203383 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 59390-149-02 | Altaire Pharmaceuticals Inc. | ANDA203383 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50090-6713-0 | A-S Medication Solutions | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 61919-392-05 | DIRECT RX | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 80425-0361-1 | Advanced Rx Pharmacy of Tennessee, LLC | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1358-2 | Taro Pharmaceuticals U.S.A., Inc. | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 55700-966-15 | Quality Care Products, LLC | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 70518-2811-0 | REMEDYREPACK INC. | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72189-319-05 | DirectRx | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 72189-454-05 | Direct_Rx | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 80425-0238-1 | Advanced Rx Pharmacy of Tennessee, LLC | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 68788-7715-1 | Preferred Pharmaceuticals, Inc. | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 71085-002-05 | IPG PHARMACEUTICALS, INC. | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 45865-118-01 | Medsource Pharmaceuticals | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 71205-062-15 | Proficient Rx LP | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 50436-3339-1 | UNIT DOSE SERVICES | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 51672-1358-4 | Taro Pharmaceuticals U.S.A., Inc. | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
MENTHOL; DICLOFENAC SODIUM | 73272-301-01 | Upstream Pharma, LLC | ANDA203818 | HUMAN PRESCRIPTION DRUG | ANDA |
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