LETROZOLE
- Product NDC
- 24724-030
- 11-digit product format
- 247240030
- Labeler code
- 24724
- Product ID
- 24724-030_f0d36846-d476-4206-99e7-51c7ae6b650a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LETROZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- INDICUS PHARMA LLC
- Application
- ANDA201804
- Marketing category
- ANDA
- Marketing start
- 2011-06-15
- 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
- 2018-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24724-030 | LETROZOLE TABLET [INDICUS PHARMA LLC] | 3 | Legacy NDC | 20110707_87b9906a-1e3f-4bd7-9f93-35d20a386315.zip |