Loratadine
- Product NDC
- 11673-527
- 11-digit product format
- 116730527
- Labeler code
- 11673
- Product ID
- 11673-527_710cd931-0ca1-45b3-a430-14237c2365f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Target Corporation
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-527-31 | Loratadine | 30 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 30 | | 3 |
| 11673-527-31 | Loratadine | 1 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 1 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-527 | LORATADINE TABLET, ORALLY DISINTEGRATING [TARGET CORPORATION] | 3 | Legacy NDC, 2 package rows | 20130424_e2fe073f-14da-424f-a34c-486d666fd649.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 11673-527-31 | 11673052731 | 30 in 1 BLISTER PACK | Historical |