cetirizine hydrochloride
- Product NDC
- 50090-4344
- 11-digit product format
- 500904344
- Labeler code
- 50090
- Product ID
- 50090-4344_ea67f1c4-964a-426d-a9fe-f061b5384e39
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA078336
- Marketing category
- ANDA
- Marketing start
- 2007-12-27
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4344-0 | 50090434400 | 14 TABLET in 1 BOTTLE (50090-4344-0) | 14 tablet | 2019-06-07 | 0000-00-00 | No | No | Current |
| 50090-4344-1 | 50090434401 | 30 TABLET in 1 BOTTLE (50090-4344-1) | 30 tablet | 2019-06-07 | 0000-00-00 | No | No | Current |
| 50090-4344-2 | 50090434402 | 100 TABLET in 1 BOTTLE (50090-4344-2) | 100 tablet | 2019-06-14 | 0000-00-00 | No | No | Current |
| 50090-4344-3 | 50090434403 | 90 TABLET in 1 BOTTLE (50090-4344-3) | 90 tablet | 2019-06-14 | 0000-00-00 | No | No | Current |