LETROZOLE
- Product NDC
- 57884-2021
- 11-digit product format
- 578842021
- Labeler code
- 57884
- Product ID
- 57884-2021_c9b165bf-73bc-0a3d-e053-2a95a90a116d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LETROZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Jiangsu Hengrui Pharmaceuticals Co., Ltd.
- Application
- ANDA202716
- Marketing category
- ANDA
- Marketing start
- 2013-05-16
- Marketing end
- 0000-00-00
- Substance
- LETROZOLE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57884-2021-1 | 57884202101 | 30 TABLET in 1 BOTTLE (57884-2021-1) | 30 tablet | 2013-05-16 | 0000-00-00 | No | No | Current |