Hydroxyzine Hydrochloride 68788-8716
Product NDC
68788-8716- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 26, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA040600
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Hydrochloride | 10 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (68788-8716-3)