Product NDC: | 52544-204 |
Proprietary Name: | GENERESS Fe |
Non Proprietary Name: | norethindrone and ethinyl estradiol and ferrous fumarate |
Active Ingredient(s): | & nbsp; norethindrone and ethinyl estradiol and ferrous fumarate |
Administration Route(s): | ORAL |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52544-204 |
Labeler Name: | Watson Pharma, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022573 |
Marketing Category: | NDA |
Start Marketing Date: | 20111223 |
Package NDC: | 52544-204-31 |
Package Description: | 3 BLISTER PACK in 1 CARTON (52544-204-31) > 1 KIT in 1 BLISTER PACK |
NDC Code | 52544-204-31 |
Proprietary Name | GENERESS Fe |
Package Description | 3 BLISTER PACK in 1 CARTON (52544-204-31) > 1 KIT in 1 BLISTER PACK |
Product NDC | 52544-204 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | norethindrone and ethinyl estradiol and ferrous fumarate |
Dosage Form Name | KIT |
Route Name | ORAL |
Start Marketing Date | 20111223 |
Marketing Category Name | NDA |
Labeler Name | Watson Pharma, Inc. |
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