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Lo Loestrin Fe
Lo Loestrin Fe - 0430-0420-14 - (norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate)
Drug Information of Lo Loestrin Fe
| Product NDC: | 0430-0420 |
| Proprietary Name: | Lo Loestrin Fe |
| Non Proprietary Name: | norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate |
| Active Ingredient(s): | & nbsp; norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Lo Loestrin Fe
| Product NDC: | 0430-0420 |
| Labeler Name: | Warner Chilcott (US), LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022501 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101201 |
Package Information of Lo Loestrin Fe
| Package NDC: | 0430-0420-14 |
| Package Description: | 5 BLISTER PACK in 1 CARTON (0430-0420-14) > 1 KIT in 1 BLISTER PACK |
NDC Information of Lo Loestrin Fe
| NDC Code | 0430-0420-14 |
| Proprietary Name | Lo Loestrin Fe |
| Package Description | 5 BLISTER PACK in 1 CARTON (0430-0420-14) > 1 KIT in 1 BLISTER PACK |
| Product NDC | 0430-0420 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20101201 |
| Marketing Category Name | NDA |
| Labeler Name | Warner Chilcott (US), LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
