Desloratadine
- Product NDC
- 63629-5270
- 11-digit product format
- 636295270
- Labeler code
- 63629
- Product ID
- 63629-5270_f1d032ff-f7fd-4cdb-a15c-8acf645fcdcd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desloratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078355
- Marketing category
- ANDA
- Marketing start
- 2012-07-01
- Marketing end
- 0000-00-00
- Substance
- DESLORATADINE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#