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 |
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MEDROXYPROGESTERONE ACETATE | 0009-0051-01 | Pharmacia & Upjohn Company LLC | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE | 0009-0065-01 | Pharmacia & Upjohn Company LLC | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE | 0009-0287-01 | Pharmacia & Upjohn Company LLC | NDA011839 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE | 0009-0746-30 | Pharmacia & Upjohn Company LLC | NDA020246 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE | 0009-0746-35 | Pharmacia & Upjohn Company LLC | NDA020246 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE | 0009-4709-13 | Pharmacia & Upjohn Company LLC | NDA021583 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE | 0009-7376-11 | Pharmacia & Upjohn Company LLC | NDA020246 | HUMAN PRESCRIPTION DRUG | NDA |
ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE | 0046-1105-11 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE; ESTROGENS, CONJUGATED | 0046-1106-11 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE | 0046-1107-11 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE | 0046-1108-11 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE; ESTROGENS, CONJUGATED | 0046-2575-12 | Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | NDA020527 | HUMAN PRESCRIPTION DRUG | NDA |
MEDROXYPROGESTERONE ACETATE | 0548-5400-00 | Amphastar Pharmaceuticals, Inc. | ANDA077235 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0548-5400-25 | Amphastar Pharmaceuticals, Inc. | ANDA077235 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0548-5410-00 | Amphastar Pharmaceuticals, Inc. | ANDA077235 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0548-5410-25 | Amphastar Pharmaceuticals, Inc. | ANDA077235 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0548-5701-00 | Amphastar Pharmaceuticals, Inc. | ANDA077334 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0548-5711-00 | Amphastar Pharmaceuticals, Inc. | ANDA077334 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0555-0779-02 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0555-0779-04 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0555-0872-02 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0555-0872-04 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0555-0873-02 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 0555-0873-04 | Teva Pharmaceuticals USA, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 10544-001-30 | Blenheim Pharmacal, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 10544-062-10 | Blenheim Pharmacal, Inc. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 21695-896-10 | Rebel Distributors Corp. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 21695-896-20 | Rebel Distributors Corp. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 21695-896-30 | Rebel Distributors Corp. | ANDA040159 | HUMAN PRESCRIPTION DRUG | ANDA |
MEDROXYPROGESTERONE ACETATE | 24201-150-00 | Hikma Pharmaceuticals USA inc. | ANDA214309 | HUMAN PRESCRIPTION DRUG | ANDA |
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