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Exemestane
Exemestane - 0054-0080-13 - (Exemestane)
Drug Information of Exemestane
| Product NDC: | 0054-0080 |
| Proprietary Name: | Exemestane |
| Non Proprietary Name: | Exemestane |
| Active Ingredient(s): | 25 mg/1 & nbsp; Exemestane |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Exemestane
| Product NDC: | 0054-0080 |
| Labeler Name: | Roxane Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077431 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110401 |
Package Information of Exemestane
| Package NDC: | 0054-0080-13 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0054-0080-13) |
NDC Information of Exemestane
| NDC Code | 0054-0080-13 |
| Proprietary Name | Exemestane |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0054-0080-13) |
| Product NDC | 0054-0080 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Exemestane |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110401 |
| Marketing Category Name | ANDA |
| Labeler Name | Roxane Laboratories, Inc |
| Substance Name | EXEMESTANE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |
