Childrens Cetirizine Hydrochloride
- Product NDC
- 68788-8992
- 11-digit product format
- 687888992
- Labeler code
- 68788
- Product ID
- 68788-8992_8c2bdc64-0775-4fe8-a42d-b8025c96690c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA090182
- Marketing category
- ANDA
- Marketing start
- 2016-02-15
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-8992-1 | 68788899201 | 120 mL in 1 BOTTLE (68788-8992-1) | 120 ml | 2016-02-15 | 0000-00-00 | No | No | Current |