Hydroxyzine Hydrochloride 11534-0206
Product NDC
11534-0206- Manufacturer
- Sunrise Pharmaceutical, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA207121
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (11534-206-01)
1000 TABLET, FILM COATED in 1 BOTTLE (11534-206-03)
500 TABLET, FILM COATED in 1 BOTTLE (11534-206-04)