Cetirizine Hydrochloride
- Product NDC
- 63629-8041
- 11-digit product format
- 636298041
- Labeler code
- 63629
- Product ID
- 63629-8041_48d61a14-3276-45e0-ba98-0e08c0b49196
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077829
- Marketing category
- ANDA
- Marketing start
- 2009-10-01
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 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 |
|---|
| 63629-8041-1 | 63629804101 | 60 TABLET in 1 BOTTLE (63629-8041-1) | 60 tablet | 2019-07-15 | 0000-00-00 | No | No | Current |