| Product NDC: | 54868-6161 |
| Proprietary Name: | FEMCON 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): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-6161 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021490 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100921 |
| Package NDC: | 54868-6161-0 |
| Package Description: | 1 BLISTER PACK in 1 CELLO PACK (54868-6161-0) > 1 KIT in 1 BLISTER PACK |
| NDC Code | 54868-6161-0 |
| Proprietary Name | FEMCON Fe |
| Package Description | 1 BLISTER PACK in 1 CELLO PACK (54868-6161-0) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 54868-6161 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone and ethinyl estradiol, and ferrous fumarate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20100921 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | |
| Strength Number | |
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