Hydroxyzine Hydrochloride 10702-0012
Product NDC
10702-0012- Manufacturer
- Kvk-Tech, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 24, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA040786
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (10702-012-01)
1000 TABLET, FILM COATED in 1 BOTTLE (10702-012-10)
500 TABLET, FILM COATED in 1 BOTTLE (10702-012-50)