Product NDC: | 54868-6100 |
Proprietary Name: | Loestrin 24 Fe |
Non Proprietary Name: | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
Active Ingredient(s): | & nbsp; norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6100 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021871 |
Marketing Category: | NDA |
Start Marketing Date: | 20100128 |
Package NDC: | 54868-6100-0 |
Package Description: | 1 BLISTER PACK in 1 POUCH (54868-6100-0) > 1 KIT in 1 BLISTER PACK |
NDC Code | 54868-6100-0 |
Proprietary Name | Loestrin 24 Fe |
Package Description | 1 BLISTER PACK in 1 POUCH (54868-6100-0) > 1 KIT in 1 BLISTER PACK |
Product NDC | 54868-6100 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | norethindrone acetate and ethinyl estradiol, and ferrous fumarate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100128 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
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