Xyzal
- Product NDC
- 0024-5803
- 11-digit product format
- 000245803
- Labeler code
- 0024
- Product ID
- 0024-5803_e96c760a-8427-4e90-a3fd-5bc091016a3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levocetirizine dihydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sanofi-Aventis U.S. LLC
- Application
- NDA022064
- Marketing category
- NDA
- Marketing start
- 2017-07-24
- Marketing end
- 0000-00-00
- Substance
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0024-5803-90 | 00024580390 | 90 TABLET, FILM COATED in 1 BOTTLE (0024-5803-90) | 2017-07-24 | 0000-00-00 | No | No | Current |