Hydroxyzine Hydrochloride 68788-8707
Product NDC
68788-8707- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA217652
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Hydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
30 TABLET, FILM COATED in 1 BOTTLE (68788-8707-3)
60 TABLET, FILM COATED in 1 BOTTLE (68788-8707-6)
90 TABLET, FILM COATED in 1 BOTTLE (68788-8707-9)