Hydroxyzine Hydrochloride 23155-0501
Product NDC
23155-0501- Manufacturer
- Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 20, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA204279
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
100 TABLET in 1 BOTTLE (23155-501-01)
500 TABLET in 1 BOTTLE (23155-501-05)
1000 TABLET in 1 BOTTLE (23155-501-10)