FDA Application
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NDC Search Results on Active Ingredient: medroxyprogesterone acetate
Click on Active Ingredient to view the label.
| Ingredient Name | NDC | Company Name | Application Number or Regulatory Citation | Product Type | Marketing Category |
|---|---|---|---|---|---|
| MEDROXYPROGESTERONE ACETATE | 63187-382-90 | Proficient Rx LP | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 54348-805-10 | PharmPak, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 10544-062-10 | Blenheim Pharmacal, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 33261-609-30 | Aidarex Pharmaceuticals LLC | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 66993-370-83 | Prasco Laboratories | NDA020246 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| MEDROXYPROGESTERONE ACETATE | 68071-4132-1 | NuCare Pharmaceuticals,Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 0548-5400-00 | Amphastar Pharmaceuticals, Inc. | ANDA077235 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 55150-329-25 | Eugia US LLC | ANDA212824 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 0555-0873-02 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 53002-3570-3 | RPK Pharmaceuticals, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 0009-0051-01 | Pharmacia & Upjohn Company LLC | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA |
| MEDROXYPROGESTERONE ACETATE | 50090-0166-0 | A-S Medication Solutions | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 24201-150-25 | Hikma Pharmaceuticals USA inc. | ANDA214309 | HUMAN PRESCRIPTION DRUG | ANDA |
| 1-30 | 31-60 | 61-90 | 91-120 | 121-133 |
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