Loratadine Allergy Relief
- Product NDC
- 64725-0526
- 11-digit product format
- 647250526
- Labeler code
- 64725
- Product ID
- 64725-0526_97284b19-ca6f-4ec0-adbc-b0720cec7e49
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- TYA Pharmaceuticals
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2003-08-28
- 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 |
|---|
| 64725-0526-1 | Loratadine Allergy Relief | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64725-0526 | LORATADINE ALLERGY RELIEF (LORATADINE) TABLET [TYA PHARMACEUTICALS] | 3 | Legacy NDC, 1 package rows | 20161207_ff1b0b4e-f74f-451d-8d13-4fa707727547.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 64725-0526-1 | 64725052601 | 100 in 1 BOTTLE | Historical |