ANASTROZOLE
- Product NDC
- 68071-3853
- 11-digit product format
- 680713853
- Labeler code
- 68071
- Product ID
- 68071-3853_4587a0ae-889c-26c8-e063-6394a90adb3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ANASTROZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA079220
- Marketing category
- ANDA
- Marketing start
- 2010-06-28
- 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 |
|---|
| 68071-3853-7 | ANASTROZOLE | 12 in 1 BOTTLE | TABLET | 12 | | 2 |
| 68071-3853-8 | ANASTROZOLE | 8 in 1 BOTTLE | TABLET | 8 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68071-3853 | ANASTROZOLE TABLET [NUCARE PHARMACEUTICALS, INC.] | 1 | Current NDC, 2 package rows | 20250529_362034e9-2830-19a5-e063-6394a90a8dfb.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 |
|---|
| 68071-3853-7 | 68071385307 | 12 TABLET in 1 BOTTLE (68071-3853-7) | 12 tablet | 2025-12-09 | No | No | Historical |
| 68071-3853-8 | 68071385308 | 8 TABLET in 1 BOTTLE (68071-3853-8) | 8 tablet | 2025-05-27 | No | No | Historical |