Cetirizine Hydrochloride 69452-0465
Product NDC
69452-0465- Manufacturer
- Bionpharma Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- October 20, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA078862
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
400 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-465-81)