Cetirizine Hydrochloride 68788-4072
Product NDC
68788-4072- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- January 27, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA078336
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(3)
1 BOTTLE in 1 CARTON (68788-4072-3) / 30 TABLET, FILM COATED in 1 BOTTLE
60 TABLET, FILM COATED in 1 BOTTLE (68788-4072-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-4072-9)