Loratadine
- Product NDC
- 56062-526
- 11-digit product format
- 560620526
- Labeler code
- 56062
- Product ID
- 56062-526_de419bf1-bd40-41df-9349-29b45b816289
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Publix Super Markets Inc
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2003-08-19
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 56062-526-31 | Loratadine | 30 in 1 BLISTER PACK | TABLET | 30 | | 3 |
| 56062-526-69 | Loratadine | 10 in 1 BLISTER PACK | TABLET | 10 | | 3 |
| 56062-526-90 | Loratadine | 90 in 1 BOTTLE | TABLET | 90 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 56062-526 | LORATADINE TABLET [PUBLIX SUPER MARKETS INC] | 3 | Legacy NDC, 3 package rows | 20190920_af62d327-791f-48c1-9200-d49b71558885.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 |
|---|
| 56062-526-31 | 56062052631 | 30 TABLET in 1 BLISTER PACK (56062-526-31) | 30 tablet | 2003-08-19 | 0000-00-00 | No | No | Current |
| 56062-526-69 | 56062052669 | 10 TABLET in 1 BLISTER PACK (56062-526-69) | 10 tablet | 2003-08-19 | 0000-00-00 | No | No | Current |
| 56062-526-90 | 56062052690 | 90 TABLET in 1 BOTTLE (56062-526-90) | 90 tablet | 2003-08-19 | 0000-00-00 | No | No | Current |