Desloratadine
- Product NDC
- 42291-240
- 11-digit product format
- 422910240
- Labeler code
- 42291
- Product ID
- 42291-240_d579fa0e-c034-3005-e053-2995a90af9a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Desloratadine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA078355
- Marketing category
- ANDA
- Marketing start
- 2015-11-24
- 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
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-240-90 | 42291024090 | 90 TABLET in 1 BOTTLE (42291-240-90) | 90 tablet | 2015-11-24 | 0000-00-00 | No | No | Current |