Hydroxyzine Hydrochloride 16571-0113
Product NDC
16571-0113- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA217652
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 10 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (16571-113-01)
500 TABLET, FILM COATED in 1 BOTTLE (16571-113-50)