Cetirizine Hydrochloride
- Product NDC
- 68788-9493
- 11-digit product format
- 687889493
- Labeler code
- 68788
- Product ID
- 68788-9493_42937ef2-f490-474b-8a81-34ce0513dcfa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cetirizine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA078488
- Marketing category
- ANDA
- Marketing start
- 2014-04-02
- Marketing end
- 0000-00-00
- Substance
- CETIRIZINE HYDROCHLORIDE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record