loratadine
- Product NDC
- 11822-0919
- 11-digit product format
- 118220919
- Labeler code
- 11822
- Product ID
- 11822-0919_754e27cd-8990-46b7-9325-16e1765c0807
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- ANDA076011
- Marketing category
- ANDA
- Marketing start
- 2020-09-25
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- loratadine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LORATADINE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 7AJO3BO7QN |
| Rxcui | 311373 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11822-0919-0 | loratadine | 1 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 1 | | 3 |
| 11822-0919-0 | loratadine | 30 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0919 | LORATADINE TABLET, ORALLY DISINTEGRATING [RITE AID CORPORATION] | 3 | Current NDC, Legacy NDC, 2 package rows | 20231224_004dd408-e3ff-4ba6-b859-beebe364f0e1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0919-0 | 11822091900 | 30 BLISTER PACK in 1 CARTON (11822-0919-0) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK | 30 blister pack | 2020-09-25 | 0000-00-00 | No | No | Current |