letrozole
- Product NDC
- 65841-744
- 11-digit product format
- 658410744
- Labeler code
- 65841
- Product ID
- 65841-744_85b17865-72d8-48a2-bb51-6d0906d075da
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- letrozole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Cadila Healthcare Limited
- Application
- ANDA090405
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- Marketing end
- 0000-00-00
- Substance
- LETROZOLE
- Active strength
- 3 mg/1
- Pharmacologic classes
- Aromatase Inhibitor [EPC],Aromatase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#