Nexesta Fe is a Kit in the Human Prescription Drug category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is .
| Product ID | 65862-926_0ff53815-ccf8-4271-8f5b-7dab45edd0d6 |
| NDC | 65862-926 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Nexesta Fe |
| Generic Name | Norethindrone And Ethinyl Estradiol And Ferrous Fumarate |
| Dosage Form | Kit |
| Marketing Start Date | 2017-02-02 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA207535 |
| Labeler Name | Aurobindo Pharma Limited |
| Active Ingredient Strength | 0 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2017-02-02 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA207535 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-02-02 |
| Marketing Category | ANDA |
| Application Number | ANDA207535 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-02-02 |
| Marketing Category | ANDA |
| Application Number | ANDA207535 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-02-02 |
| Marketing Category | ANDA |
| Application Number | ANDA207535 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2017-02-02 |
| SPL SET ID: | 6eb8f7b6-4b8e-4bad-800a-b2f3b36c3413 |
| Manufacturer | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 65862-926 | Nexesta Fe | norethindrone and ethinyl estradiol and ferrous fumarate |
| 0023-6030 | GENERESS Fe | norethindrone and ethinyl estradiol and ferrous fumarate |
| 52544-204 | GENERESS Fe | norethindrone and ethinyl estradiol and ferrous fumarate |
| 0378-7297 | NORETHINDRONE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE | norethindrone and ethinyl estradiol and ferrous fumarate |
| 0378-7308 | NORETHINDRONE AND ETHINYL ESTRADIOL AND FERROUS FUMARATE | norethindrone and ethinyl estradiol and ferrous fumarate |