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 | 72275-707-77 | Primary Pharmaceuticals, Inc. | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
LIDOCAINE HYDROCHLORIDE; DICLOFENAC SODIUM | 80425-0330-1 | Advanced Rx Pharmacy of Tennessee, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 82213-002-01 | Noor Brands Company, LLC | HUMAN OTC DRUG | unapproved drug other | |
DICLOFENAC SODIUM; LEFLUNOMIDE | 72835-602-02 | V2 Pharma, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; LIDOCAINE | 80425-0250-1 | Advanced Rx Pharmacy of Tennessee, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 59088-709-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; MENTHOL; CAPSAICIN | 72275-734-77 | Primary Pharmaceuticals, Inc | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; LIDOCAINE | 72189-390-35 | Direct_Rx | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 50335-0020-1 | Henan Dongtai Pharm Co., Ltd. | BULK INGREDIENT | bulk ingredient for animal drug compounding | |
HYALURONATE SODIUM; CALCIPOTRIENE; DICLOFENAC SODIUM; NIACINAMIDE | 72934-2030-2 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; METHYL SALICYLATE; MENTHOL | 72835-202-02 | V2 Pharma, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; CAMPHOR (SYNTHETIC); MENTHOL | 59088-785-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
LIDOCAINE; DICLOFENAC SODIUM | 53225-1070-1 | Terrain Pharmaceuticals | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 59088-727-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 82213-002-03 | Noor Brands Company, LLC | HUMAN OTC DRUG | unapproved drug other | |
CAPSAICIN; DICLOFENAC SODIUM | 81877-645-12 | FORREAL PHARMACEUTICALS LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 73377-113-01 | AX Pharmaceutical Corp | BULK INGREDIENT | bulk ingredient for animal drug compounding | |
DICLOFENAC SODIUM | 59088-365-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
LIDOCAINE HYDROCHLORIDE; DICLOFENAC SODIUM | 53225-1076-1 | Terrain Pharmaceuticals | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 69621-300-01 | Shoreline Pharmaceuticals, Inc. | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; CAPSICUM OLEORESIN | 59088-093-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; CAPSICUM OLEORESIN | 59088-784-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 82213-002-02 | Noor Brands Company, LLC | HUMAN OTC DRUG | unapproved drug other | |
MENTHOL; DICLOFENAC SODIUM; CAMPHOR (SYNTHETIC) | 59088-716-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM; CAPSICUM OLEORESIN | 59088-343-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 72934-1072-2 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
CAPSICUM OLEORESIN; DICLOFENAC SODIUM | 59088-801-00 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 76074-501-11 | Two Hip Consulting, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
DICLOFENAC SODIUM | 68151-2481-0 | Carilion Materials Management | ANDA074376 | HUMAN PRESCRIPTION DRUG | ANDA |
DICLOFENAC SODIUM | 70882-115-30 | Cambridge Therapeutics Technologies, LLC | ANDA074394 | HUMAN PRESCRIPTION DRUG | ANDA |
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