LEVOCETIRIZINE DIHYDROCHLORIDE
- Product NDC
- 63629-8069
- 11-digit product format
- 636298069
- Labeler code
- 63629
- Product ID
- 63629-8069_1314efd0-a0a7-4518-85d0-607fd1e4c2af
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOCETIRIZINE DIHYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205564
- Marketing category
- ANDA
- Marketing start
- 2016-01-11
- 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
- 2020-12-31
- 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 |
|---|
| 63629-8069-1 | 63629806901 | 90 TABLET, FILM COATED in 1 BOTTLE (63629-8069-1) | 2019-07-18 | 0000-00-00 | No | No | Current |