Cetirizine Hydrochloride
- Product NDC
- 71335-0028
- 11-digit product format
- 713350028
- Labeler code
- 71335
- Product ID
- 71335-0028_1bdc3b5b-ec66-42fd-857c-d1f91e1ad352
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077946
- 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
- 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 |
|---|
| 71335-0028-1 | 71335002801 | 30 TABLET in 1 BOTTLE (71335-0028-1) | 30 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-2 | 71335002802 | 14 TABLET in 1 BOTTLE (71335-0028-2) | 14 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-3 | 71335002803 | 7 TABLET in 1 BOTTLE (71335-0028-3) | 7 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-4 | 71335002804 | 10 TABLET in 1 BOTTLE (71335-0028-4) | 10 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-5 | 71335002805 | 15 TABLET in 1 BOTTLE (71335-0028-5) | 15 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-6 | 71335002806 | 90 TABLET in 1 BOTTLE (71335-0028-6) | 90 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-7 | 71335002807 | 20 TABLET in 1 BOTTLE (71335-0028-7) | 20 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-8 | 71335002808 | 60 TABLET in 1 BOTTLE (71335-0028-8) | 60 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |
| 71335-0028-9 | 71335002809 | 100 TABLET in 1 BOTTLE (71335-0028-9) | 100 tablet | 2010-04-02 | 0000-00-00 | No | No | Current |