FDA Application
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NDC Search Results on Active Ingredient: hydrocortisone
Click on Active Ingredient to view the label.
| Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| HYDROCORTISONE BUTYRATE | 68682-384-60 | Oceanside Pharmaceuticals | NDA020769 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| HYDROCORTISONE | 60687-582-11 | American Health Packaging | ANDA207029 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 77052-010-01 | Derm Ventures LLC | ANDA083231 | HUMAN PRESCRIPTION DRUG | ANDA |
| LIDOCAINE HYDROCHLORIDE; HYDROCORTISONE ACETATE | 59088-816-24 | PureTek Corporation | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| HYDROCORTISONE | 68462-464-17 | Glenmark Pharmaceuticals Inc., USA | ANDA202145 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE ACETATE | 63629-1994-1 | Bryant Ranch Prepack | HUMAN PRESCRIPTION DRUG | Unapproved drug other | |
| HYDROCORTISONE ACETATE; LIDOCAINE HYDROCHLORIDE | 13925-164-20 | Seton Pharmaceuticals | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| HYDROCORTISONE | 0316-0193-30 | Crown Laboratories | ANDA080706 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 71863-111-50 | Eton Pharmaceuticals, Inc. | NDA213876 | HUMAN PRESCRIPTION DRUG | NDA |
| HYDROCORTISONE | 50268-406-11 | AvPAK | ANDA040646 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 66267-967-01 | NuCare Pharmaceuticals,Inc. | ANDA085025 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE ACETATE | 10135-751-12 | Marlex Pharmaceuticals, Inc. | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| HYDROCORTISONE VALERATE | 21922-007-04 | Encube Ethicals Private Limited | ANDA211047 | HUMAN PRESCRIPTION DRUG | ANDA |
| PRAMOXINE HYDROCHLORIDE; HYDROCORTISONE ACETATE | 54766-778-04 | Sebela Pharmaceuticals Inc. | ANDA085368 | HUMAN PRESCRIPTION DRUG | ANDA |
| POLYMYXIN B SULFATE; HYDROCORTISONE; NEOMYCIN SULFATE | 61314-641-75 | Sandoz Inc | ANDA062874 | HUMAN PRESCRIPTION DRUG | ANDA |
| NEOMYCIN SULFATE; HYDROCORTISONE; POLYMYXIN B SULFATE | 53002-9001-1 | RPK Pharmaceuticals, Inc. | ANDA062488 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE; TRETINOIN; HYDROQUINONE | 72934-6226-2 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| HYDROCORTISONE | 50268-407-15 | AvPAK | ANDA040646 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 68788-8583-2 | Preferred Pharmaceuticals Inc. | ANDA088799 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE BUTYRATE | 68682-271-15 | Oceanside Pharmaceuticals | NDA018652 | HUMAN PRESCRIPTION DRUG | NDA |
| TRETINOIN; HYDROCORTISONE; HYDROQUINONE | 72934-6225-2 | Sincerus Florida, LLC | HUMAN PRESCRIPTION DRUG | unapproved drug other | |
| NEOMYCIN SULFATE; POLYMYXIN B SULFATE; HYDROCORTISONE | 63187-568-10 | Proficient Rx LP | ANDA062423 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE ACETATE | 50090-5736-0 | A-S Medication Solutions | HUMAN PRESCRIPTION DRUG | Unapproved drug other | |
| HYDROCORTISONE | 53217-197-01 | Aidarex Pharmaceuticals LLC | ANDA085025 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 63629-8847-1 | Bryant Ranch Prepack | ANDA040879 | HUMAN PRESCRIPTION DRUG | ANDA |
| PRAMOXINE HYDROCHLORIDE; HYDROCORTISONE ACETATE | 54766-726-75 | Sebela Pharmaceuticals Inc. | ANDA085979 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 0316-0128-16 | Crown Laboratories | ANDA080706 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 63629-8667-1 | Bryant Ranch Prepack | ANDA085025 | HUMAN PRESCRIPTION DRUG | ANDA |
| POLYMYXIN B SULFATE; HYDROCORTISONE; NEOMYCIN SULFATE | 70518-0763-0 | REMEDYREPACK INC. | ANDA064053 | HUMAN PRESCRIPTION DRUG | ANDA |
| HYDROCORTISONE | 72162-1383-7 | Bryant Ranch Prepack | ANDA085027 | HUMAN PRESCRIPTION DRUG | ANDA |
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