Home
>
National Drug Code (NDC)
>
EXEMESTANE
EXEMESTANE - 59762-2858-1 - (EXEMESTANE)
Drug Information of EXEMESTANE
| Product NDC: | 59762-2858 |
| Proprietary Name: | EXEMESTANE |
| Non Proprietary Name: | EXEMESTANE |
| Active Ingredient(s): | 25 mg/1 & nbsp; EXEMESTANE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, SUGAR COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of EXEMESTANE
| Product NDC: | 59762-2858 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020753 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20110401 |
Package Information of EXEMESTANE
| Package NDC: | 59762-2858-1 |
| Package Description: | 30 TABLET, SUGAR COATED in 1 BOTTLE (59762-2858-1) |
NDC Information of EXEMESTANE
| NDC Code | 59762-2858-1 |
| Proprietary Name | EXEMESTANE |
| Package Description | 30 TABLET, SUGAR COATED in 1 BOTTLE (59762-2858-1) |
| Product NDC | 59762-2858 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EXEMESTANE |
| Dosage Form Name | TABLET, SUGAR COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | EXEMESTANE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |
