Hydroxyzine Hydrochloride 68071-4499
Product NDC
68071-4499- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 19, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA088617
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 10 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (68071-4499-3)