Exemestane
- Product NDC
- 63629-2056
- 11-digit product format
- 636292056
- Labeler code
- 63629
- Product ID
- 63629-2056_24b13a97-81f9-47f1-8c49-64e63ea12bd4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Exemestane
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA211031
- Marketing category
- ANDA
- Marketing start
- 2019-12-19
- Substance
- EXEMESTANE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC], Aromatase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Exemestane
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| EXEMESTANE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | NY22HMQ4BX |
| Rxcui | 310261 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-2056-1 | Exemestane | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 104 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2056 | EXEMESTANE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 104 | Current NDC, Legacy NDC, 1 package rows | 20240601_1841ec12-3f4f-4b87-b719-fd0b4d9eaffb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2056-1 | 63629205601 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-2056-1) | 2019-12-19 | 0000-00-00 | No | No | Current |