Childrens Cetirizine Hydrochloride Allergy
- Product NDC
- 65862-422
- 11-digit product format
- 658620422
- Labeler code
- 65862
- Product ID
- 65862-422_7c93cda5-d5c5-45af-b5cd-cdb63870808a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Aurobindo Pharma Limited
- Application
- ANDA090750
- Marketing category
- ANDA
- Marketing start
- 2010-02-02
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record