Anastrozole
- Product NDC
- 24979-725
- 11-digit product format
- 249790725
- Labeler code
- 24979
- Product ID
- 24979-725_398a1cb9-25cd-a30d-e063-6394a90a1956
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole Tablets
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Upsher-Smith Laboratories, LLC
- Application
- ANDA206037
- Marketing category
- ANDA
- Marketing start
- 2025-03-21
- Substance
- ANASTROZOLE
- Active strength
- 1 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
- Anastrozole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ANASTROZOLE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 2Z07MYW1AZ |
| Rxcui | 199224 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24979-725-06 | Anastrozole | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 24979-725-07 | Anastrozole | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24979-725 | ANASTROZOLE (ANASTROZOLE TABLETS) TABLET [UPSHER-SMITH LABORATORIES, LLC] | 1 | Current NDC, 2 package rows | 20250313_7e0bd2cc-d3cc-403f-a6b6-4597ccb2f685.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 24979-725-06 | 24979072506 | 30 TABLET in 1 BOTTLE (24979-725-06) | 30 tablet | 2025-03-21 | No | No | Historical |
| 24979-725-07 | 24979072507 | 90 TABLET in 1 BOTTLE (24979-725-07) | 90 tablet | 2025-03-21 | No | No | Historical |