NDC 71921-190
Exemestane
Exemestane
Exemestane is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Florida Pharmaceutical Products, Llc. The primary component is Exemestane.
| Product ID | 71921-190_19609404-4c6f-4037-b5e3-3619bda20bdb |
| NDC | 71921-190 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Exemestane |
| Generic Name | Exemestane |
| Dosage Form | Tablet, Film Coated |
| Route of Administration | ORAL |
| Marketing Start Date | 2021-01-15 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA213547 |
| Labeler Name | Florida Pharmaceutical Products, LLC |
| Substance Name | EXEMESTANE |
| Active Ingredient Strength | 25 mg/1 |
| Pharm Classes | Aromatase Inhibitor [EPC], Aromatase Inhibitors [MoA] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |