Hydroxyzine Hydrochloride 42806-0159
Product NDC
42806-0159- Manufacturer
- Epic Pharma, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 31, 2015
- Listing Expires
- December 31, 2026
- Application
- ANDA040604
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 10 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (42806-159-01)
500 TABLET, FILM COATED in 1 BOTTLE (42806-159-05)
1000 TABLET, FILM COATED in 1 BOTTLE (42806-159-10)