Loratadine
- Product NDC
- 17856-6234
- 11-digit product format
- 178566234
- Labeler code
- 17856
- Product ID
- 17856-6234_ccf9ac38-566e-4fe2-86c7-0b62b52153fc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- ANDA077421
- Marketing category
- ANDA
- Marketing start
- 2011-02-17
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 17856-6234-2 | Loratadine | 5 mL in 1 CUP | SOLUTION | 5 | | 3 |
| 17856-6234-5 | Loratadine | 5 mL in 1 CUP | SOLUTION | 5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-6234 | LORATADINE (LORATADINE) SOLUTION [ATLANTIC BIOLOGICALS CORPS] | 3 | Legacy NDC, 2 package rows | 20160816_5a443fa3-a38f-4e4e-b6a0-7773a3d5ec83.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-6234-2 | 17856623402 | 5 mL in 1 CUP | 5 ml | Historical |
| 17856-6234-5 | 17856623405 | 5 mL in 1 CUP | 5 ml | Historical |