Desloratadine
- Product NDC
- 51672-4159
- 11-digit product format
- 516724159
- Labeler code
- 51672
- Product ID
- 51672-4159_4e3d4c62-ca09-4a45-8fe8-0faccb492037
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desloratadine
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Taro Pharmaceuticals U.S.A., Inc.
- Application
- ANDA202592
- Marketing category
- ANDA
- Marketing start
- 2015-07-01
- Marketing end
- 0000-00-00
- Substance
- DESLORATADINE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record