Loratadine
- Product NDC
- 50090-3464
- 11-digit product format
- 500903464
- Labeler code
- 50090
- Product ID
- 50090-3464_4a1853f2-77cd-475e-93db-d6da97f27fcf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA075209
- Marketing category
- ANDA
- Marketing start
- 2016-02-01
- 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 |
|---|
| 50090-3464-0 | Loratadine | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-3464 | LORATADINE TABLET [A-S MEDICATION SOLUTIONS] | 1 | Legacy NDC, 1 package rows | 20190205_0c5a71f2-ffec-47aa-8283-6297a02c7581.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 |
|---|
| 50090-3464-0 | 50090346400 | 30 TABLET in 1 BOTTLE (50090-3464-0) | 30 tablet | 2018-05-29 | 0000-00-00 | No | No | Current |