Letrozole
- Product NDC
- 60505-3255
- 11-digit product format
- 605053255
- Labeler code
- 60505
- Product ID
- 60505-3255_e055b181-3341-1886-a9c1-0c552a9a18a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Letrozole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA091303
- Marketing category
- ANDA
- Marketing start
- 2012-05-31
- Marketing end
- 2021-12-31
- Substance
- LETROZOLE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-3255-3 | 60505325503 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-3255-3) | 2012-05-31 | 2021-12-31 | No | No | Current |