LETROZOLE
- Product NDC
- 24535-0801
- 11-digit product format
- 245350801
- Labeler code
- 24535
- Product ID
- 24535-0801_b826b788-446f-49c9-bca2-2a3e7bbc43eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LETROZOLE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Arab Pharmaceutical Manufacturing Co. PSC Ltd
- Application
- ANDA203796
- Marketing category
- ANDA
- Marketing start
- 2016-06-03
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 24535-0801-1 | LETROZOLE | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 24535-0801 | LETROZOLE TABLET, FILM COATED [ARAB PHARMACEUTICAL MANUFACTURING CO. PSC LTD] | 3 | Legacy NDC, 1 package rows | 20160629_968611f1-ef03-47a6-8dae-4834f77d23bd.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 24535-0801-1 | 24535080101 | 30 in 1 BOTTLE | Historical |