Hydroxyzine Hydrochloride 70954-0912
Product NDC
70954-0912- Manufacturer
- Ani Pharmaceuticals, Inc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 15, 2026
- Listing Expires
- December 31, 2026
- Application
- ANDA219648
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 10 mg/5mL |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
473 mL in 1 BOTTLE (70954-912-10)