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Aromasin
Aromasin - 0009-7663-04 - (EXEMESTANE)
Drug Information of Aromasin
| Product NDC: | 0009-7663 |
| Proprietary Name: | Aromasin |
| Non Proprietary Name: | EXEMESTANE |
| Active Ingredient(s): | 25 mg/1 & nbsp; EXEMESTANE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aromasin
| Product NDC: | 0009-7663 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020753 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19991021 |
Package Information of Aromasin
| Package NDC: | 0009-7663-04 |
| Package Description: | 30 TABLET in 1 BOTTLE (0009-7663-04) |
NDC Information of Aromasin
| NDC Code | 0009-7663-04 |
| Proprietary Name | Aromasin |
| Package Description | 30 TABLET in 1 BOTTLE (0009-7663-04) |
| Product NDC | 0009-7663 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EXEMESTANE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19991021 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | EXEMESTANE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA] |
