Cetrizine Hydrochloride
- Product NDC
- 0904-6372
- 11-digit product format
- 009046372
- Labeler code
- 0904
- Product ID
- 0904-6372_7f720ea2-ce48-46fd-e053-2991aa0a71ea
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- CETIRIZINE HYDROCHLORIDE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA090474
- Marketing category
- ANDA
- Marketing start
- 2014-02-24
- 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