Hydroxyzine Hydrochloride 68788-7854
Product NDC
68788-7854- Manufacturer
- Preferred Pharmaceuticals Incl
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 29, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA204279
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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 in 1 BOTTLE (68788-7854-3)
60 TABLET in 1 BOTTLE (68788-7854-6)
90 TABLET in 1 BOTTLE (68788-7854-9)