Letrozole
- Product NDC
- 68071-2167
- 11-digit product format
- 680712167
- Labeler code
- 68071
- Product ID
- 68071-2167_1b409bb6-209f-1ce8-e063-6394a90ac12a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- letrozole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA090934
- Marketing category
- ANDA
- Marketing start
- 2011-06-02
- Substance
- LETROZOLE
- Active strength
- 2.5 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 |
|---|
| 7LKK855W8I | LETROZOLE | 112809-51-5 | LETROZOLE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-2167-4 | 68071216704 | 40 TABLET, FILM COATED in 1 BOTTLE (68071-2167-4) | 2024-06-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Letrozole | NuCare Pharmaceuticals,Inc. | 2024-06-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |