Childrens Cetirizine Hydrochloride
- Product NDC
- 62011-0093
- 11-digit product format
- 620110093
- Labeler code
- 62011
- Product ID
- 62011-0093_204a967a-0742-4b0a-9a24-e0ee7e44479b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Cetirizine hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Health Mart
- Application
- ANDA201546
- Marketing category
- ANDA
- Marketing start
- 2011-05-20
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#