Loratadine
- Product NDC
- 41520-513
- 11-digit product format
- 415200513
- Labeler code
- 41520
- Product ID
- 41520-513_b9692ba4-8ebc-40db-a9e0-87a4369f5fc1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- American Sales Company
- Application
- ANDA077153
- Marketing category
- ANDA
- Marketing start
- 2007-08-31
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 41520-513-24 | Loratadine | 24 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 24 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41520-513 | LORATADINE TABLET, ORALLY DISINTEGRATING [AMERICAN SALES COMPANY] | 1 | Legacy NDC, 1 package rows | 20130214_04a54364-7f13-4b23-8445-9cbc57733e18.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 41520-513-24 | 41520051324 | 24 in 1 BLISTER PACK | Historical |