Loratadine
- Product NDC
- 68788-9805
- 11-digit product format
- 687889805
- Labeler code
- 68788
- Product ID
- 68788-9805_77cdd926-45d3-46d9-be75-aef8a33f6af6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Loratadine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA077421
- Marketing category
- ANDA
- Marketing start
- 2012-05-09
- Marketing end
- 0000-00-00
- Substance
- LORATADINE
- Active strength
- 5 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record