Loratadine OD
- Product NDC
- 55315-529
- 11-digit product format
- 553150529
- Labeler code
- 55315
- Product ID
- 55315-529_cf0be8c3-50d2-4b7f-8120-33754890e2b2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Fred's Inc.
- 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
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55315-529-31 | Loratadine OD | 30 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55315-529 | LORATADINE OD (LORATADINE) TABLET, ORALLY DISINTEGRATING [FRED'S INC.] | 1 | Legacy NDC, 1 package rows | 20130211_5f246f7a-a221-49d1-94cb-526e0685f48c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 55315-529-31 | 55315052931 | 30 in 1 BLISTER PACK | Historical |