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GENERESS Fe
GENERESS Fe - 52544-204-31 - (norethindrone and ethinyl estradiol and ferrous fumarate)
Drug Information of GENERESS Fe
| 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) |
Labeler Information of GENERESS Fe
| 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 Information of GENERESS Fe
| Package NDC: | 52544-204-31 |
| Package Description: | 3 BLISTER PACK in 1 CARTON (52544-204-31) > 1 KIT in 1 BLISTER PACK |
NDC Information of GENERESS Fe
| 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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