Hydroxyzine Hydrochloride 80425-0376
Product NDC
80425-0376- Manufacturer
- Advanced Rx Pharmacy Of Tennessee, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 13, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA087871
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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 (80425-0376-1)
60 TABLET, FILM COATED in 1 BOTTLE (80425-0376-2)