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 | 73377-133-01 | AX Pharmaceutical Corp | BULK INGREDIENT | bulk ingredient for animal drug compounding | |
| MEDROXYPROGESTERONE ACETATE | 73309-381-01 | BLUEBAY SHANDONG CO.,LTD | BULK INGREDIENT - ANIMAL DRUG | bulk ingredient for animal drug compounding | |
| MEDROXYPROGESTERONE ACETATE | 33261-534-05 | Aidarex Pharmaceuticals LLC | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 70121-1467-2 | Amneal Pharmaceuticals LLC | ANDA215397 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 60687-105-21 | American Health Packaging | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 63629-8824-1 | Bryant Ranch Prepack | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 33261-534-10 | Aidarex Pharmaceuticals LLC | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 0009-0746-30 | Pharmacia & Upjohn Company LLC | NDA020246 | HUMAN PRESCRIPTION DRUG | NDA |
| MEDROXYPROGESTERONE ACETATE | 50090-0491-1 | A-S Medication Solutions | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 0555-0872-04 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE; ESTROGENS, CONJUGATED | 0046-2575-12 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
| MEDROXYPROGESTERONE ACETATE; ESTROGENS, CONJUGATED | 68258-5980-2 | Dispensing Solutions, Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
| MEDROXYPROGESTERONE ACETATE | 68788-9899-1 | Preferred Pharmaceuticals, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 63629-2612-3 | Bryant Ranch Prepack | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 50090-0166-2 | A-S Medication Solutions | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 0555-0872-02 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 33261-740-28 | Aidarex Pharmaceuticals LLC | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE | 0046-1105-11 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
| MEDROXYPROGESTERONE ACETATE | 68071-4132-3 | NuCare Pharmaceuticals,Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 68788-9233-1 | Preferred Pharmaceuticals Inc. | NDA020246 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE | 68258-5978-2 | Dispensing Solutions, Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
| MEDROXYPROGESTERONE ACETATE | 69189-3740-1 | Avera McKennan Hospital | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| MEDROXYPROGESTERONE ACETATE | 59762-0058-2 | Greenstone LLC | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
| MEDROXYPROGESTERONE ACETATE | 63629-2612-5 | Bryant Ranch Prepack | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 55289-160-10 | PD-Rx Pharmaceuticals, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 69189-3741-1 | Avera McKennan Hospital | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA AUTHORIZED GENERIC |
| MEDROXYPROGESTERONE ACETATE | 60687-105-11 | American Health Packaging | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 0009-0065-01 | Pharmacia & Upjohn Company LLC | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA |
| MEDROXYPROGESTERONE ACETATE | 66336-603-20 | Dispensing Solutions, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
| MEDROXYPROGESTERONE ACETATE | 59762-0058-1 | Greenstone LLC | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA authorized generic |
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