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 |