Fexofenadine is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Directrx. The primary component is Fexofenadine Hydrochloride.
| Product ID | 72189-305_d35a5ce4-cd84-5b1f-e053-2995a90a24db |
| NDC | 72189-305 |
| Product Type | Human Otc Drug |
| Proprietary Name | Fexofenadine |
| Generic Name | Fexofenadine |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-12-17 |
| Marketing Category | ANDA / |
| Application Number | ANDA204097 |
| Labeler Name | DirectRx |
| Substance Name | FEXOFENADINE HYDROCHLORIDE |
| Active Ingredient Strength | 180 mg/1 |
| NDC Exclude Flag | N |
| Listing Certified Through | 2022-12-31 |
| Marketing Start Date | 2021-12-17 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 55648-744 | Fexofenadine | Fexofenadine |
| 55648-982 | Fexofenadine | Fexofenadine |
| 55648-987 | Fexofenadine | Fexofenadine |
| 64679-744 | Fexofenadine | Fexofenadine |
| 64679-982 | Fexofenadine | Fexofenadine |
| 64679-987 | Fexofenadine | Fexofenadine |
| 72189-305 | Fexofenadine | Fexofenadine |
| 0378-0781 | Fexofenadine Hydrochloride | fexofenadine |
| 0378-0782 | Fexofenadine Hydrochloride | fexofenadine |
| 0615-7696 | Fexofenadine Hydrochloride | Fexofenadine |
| 43353-760 | Fexofenadine Hydrochloride | fexofenadine |
| 70518-0746 | Fexofenadine Hydrochloride | fexofenadine |
| 0615-7695 | Fexofenodine Hydrochloride | Fexofenadine |