Anastrozole
- Product NDC
- 72789-342
- 11-digit product format
- 727890342
- Labeler code
- 72789
- Product ID
- 72789-342_2e80f27e-47c5-0ddc-e063-6294a90a089c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Anastrozole
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA078921
- Marketing category
- ANDA
- Marketing start
- 2010-06-27
- 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 |
|---|
| 72789-342-15 | Anastrozole | 15 in 1 BOTTLE, PLASTIC | TABLET, COATED | 15 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72789-342 | ANASTROZOLE TABLET, COATED [PD-RX PHARMACEUTICALS, INC.] | 16 | Current NDC, 1 package rows | 20250221_b023a9f2-1a99-4b40-a953-edac7e3a79bf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-342-15 | 72789034215 | 15 TABLET, COATED in 1 BOTTLE, PLASTIC (72789-342-15) | 2023-09-01 | No | No | Historical |