ANASTROZOLE
- Product NDC
- 68071-3838
- 11-digit product format
- 680713838
- Labeler code
- 68071
- Product ID
- 68071-3838_33f146ec-fefc-c9b8-e063-6294a90ac588
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 2Z07MYW1AZ | ANASTROZOLE | 120511-73-1 | ANASTROZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3838-9 | 68071383809 | 90 TABLET in 1 BOTTLE (68071-3838-9) | 90 tablet | 2025-04-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ANASTROZOLE | NuCare Pharmaceuticals,Inc. | 2025-04-29 | HUMAN PRESCRIPTION DRUG LABEL | 1 |