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 |