Loratadine Allergy Relief
- Product NDC
- 71141-132
- 11-digit product format
- 711410132
- Labeler code
- 71141
- Product ID
- 71141-132_059bf46f-8a79-486a-995f-5f4e986ea178
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- LIDL US, LLC
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2017-09-01
- 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 Allergy Relief
- 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 | 311372 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71141-132-32 | Loratadine Allergy Relief | 10 in 1 BLISTER PACK | TABLET | 10 | | 1 |
| 71141-132-32 | Loratadine Allergy Relief | 1 in 1 CARTON | TABLET | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71141-132 | LORATADINE ALLERGY RELIEF (LORATADINE) TABLET [LIDL US, LLC] | 1 | Current NDC, Legacy NDC, 2 package rows | 20180110_11bc027c-d28d-45f0-a4cb-24a3834a6995.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 |
|---|
| 71141-132-32 | 71141013232 | 1 BLISTER PACK in 1 CARTON (71141-132-32) / 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2017-09-01 | 0000-00-00 | No | No | Current |