Hydroxyzine Hydrochloride 68071-5291
Product NDC
68071-5291- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA217652
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
30 TABLET, FILM COATED in 1 BOTTLE (68071-5291-3)