Cetirizine Hydrochloride 48433-0017
Product NDC
48433-0017- Manufacturer
- Safecor Health, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- April 17, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA076677
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
100 BLISTER PACK in 1 CARTON (48433-017-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-017-01)