Hydroxyzine Hydrochloride 80425-0394
Product NDC
80425-0394- Manufacturer
- Advanced Rx Of Tennessee, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 24, 2024
- Listing Expires
- December 31, 2026
- 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(2)
30 TABLET, FILM COATED in 1 BOTTLE (80425-0394-1)
60 TABLET, FILM COATED in 1 BOTTLE (80425-0394-2)