Loratadine
- Product NDC
- 41163-528
- 11-digit product format
- 411630528
- Labeler code
- 41163
- Product ID
- 41163-528_35af7285-9558-4f37-a826-594676f46763
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Supervalu Inc.
- Application
- ANDA077153
- Marketing category
- ANDA
- Marketing start
- 2013-12-03
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 41163-528-31 | Loratadine | 3 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 3 | | 1 |
| 41163-528-31 | Loratadine | 10 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 10 | | 1 |
| 41163-528-69 | Loratadine | 10 in 1 BLISTER PACK | TABLET, ORALLY DISINTEGRATING | 10 | | 1 |
| 41163-528-69 | Loratadine | 1 in 1 CARTON | TABLET, ORALLY DISINTEGRATING | 1 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41163-528 | LORATADINE TABLET, ORALLY DISINTEGRATING [SUPERVALU INC.] | 1 | Legacy NDC, 4 package rows | 20131205_bc253aa7-686c-40e6-affa-a585b465046a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 41163-528-31 | 41163052831 | 3 in 1 CARTON | Historical |
| 41163-528-69 | 41163052869 | 10 in 1 BLISTER PACK | Historical |