Exemestane
- Product NDC
- 65162-240
- 11-digit product format
- 651620240
- Labeler code
- 65162
- Product ID
- 65162-240_8041371e-357b-4d85-8209-00485866b492
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Exemestane
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals LLC
- Application
- ANDA206421
- Marketing category
- ANDA
- Marketing start
- 2018-12-29
- Marketing end
- 0000-00-00
- Substance
- EXEMESTANE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC], Aromatase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 65162-240 | EXEMESTANE TABLET, FILM COATED [AMNEAL PHARMACEUTICALS LLC] | 15 | Legacy NDC | 20250108_11d5a86e-7861-43f1-ae04-84daa0de7888.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 65162-240-03 | 65162024003 | 30 TABLET, FILM COATED in 1 BOTTLE (65162-240-03) | 2018-12-29 | 0000-00-00 | No | No | Current |