Allergy Relief
- Product NDC
- 81522-393
- 11-digit product format
- 815220393
- Labeler code
- 81522
- Product ID
- 81522-393_f212641c-ab8f-62ff-e053-2a95a90a626e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- FSA STORE INC.
- Application
- ANDA210722
- Marketing category
- ANDA
- Marketing start
- 2023-01-11
- 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
- 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 |
|---|
| 81522-393-11 | Allergy Relief | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | | 2 |
| 81522-393-11 | Allergy Relief | 1 in 1 CARTON | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81522-393 | ALLERGY RELIEF (LORATADINE) TABLET [FSA STORE INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20230113_ec6b31f3-ee68-1fbc-e053-2a95a90a05aa.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 81522-393-11 | 81522039311 | 1 BOTTLE, PLASTIC in 1 CARTON (81522-393-11) / 90 TABLET in 1 BOTTLE, PLASTIC | 2023-01-11 | 0000-00-00 | No | No | Current |