Loratadine
- Product NDC
- 51660-209
- 11-digit product format
- 516600209
- Labeler code
- 51660
- Product ID
- 51660-209_79cfee1c-0ae1-40dd-92d8-cb55dff96545
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Ohm Laboratories Inc.
- Application
- ANDA076134
- Marketing category
- ANDA
- Marketing start
- 2009-06-23
- 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 |
|---|
| 51660-209-69 | Loratadine | 1 in 1 CARTON | TABLET | 1 | | 1 |
| 51660-209-69 | Loratadine | 10 in 1 BLISTER PACK | TABLET | 10 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51660-209 | LORATADINE TABLET [OHM LABORATORIES INC.] | 1 | Legacy NDC, 2 package rows | 20130924_6e22813e-d8e7-4a91-b510-50fc3f028933.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 51660-209-69 | 51660020969 | 1 in 1 CARTON | Historical |