Hydroxyzine Hydrochloride 00121-1034
Product NDC
00121-1034- Manufacturer
- Pai Holdings, Llc Dba Pai Pharma
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 10, 2002
- Listing Expires
- December 31, 2026
- Application
- ANDA040391
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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 (0121-1034-16)