Lo Loestrin Fe is a Kit in the Human Prescription Drug category. It is labeled and distributed by Allergan, Inc.. The primary component is .
| Product ID | 0430-0420_1773b726-bbc6-4821-8994-78f666ee3b70 |
| NDC | 0430-0420 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Lo Loestrin Fe |
| Generic Name | Norethindrone Acetate And Ethinyl Estradiol, Ethinyl Estradiol And Ferrous Fumarate |
| Dosage Form | Kit |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | NDA / NDA |
| Application Number | NDA022501 |
| Labeler Name | Allergan, Inc. |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |
| Marketing Start Date | 2010-12-01 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA022501 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | NDA |
| Application Number | NDA022501 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2010-12-01 |
| Marketing Category | NDA |
| Application Number | NDA022501 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2010-12-01 |
| SPL SET ID: | c33072cf-625d-4b4a-981e-ec049c5d78aa |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 0430-0420 | Lo Loestrin Fe | norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate |
| 50090-1456 | Lo Loestrin Fe | norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate |
| 0430-0537 | Lo Minastrin Fe | norethindrone acetate and ethinyl estradiol, ethinyl estradiol and ferrous fumarate |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() LO LOESTRIN FE 97900357 not registered Live/Pending |
Barr Laboratories, Inc. 2023-04-21 |
![]() LO LOESTRIN FE 85198440 4015290 Live/Registered |
ALLERGAN PHARMACEUTICALS INTERNATIONAL LIMITED 2010-12-15 |