Hydroxyzine Hydrochloride 10135-0812
Product NDC
10135-0812- Manufacturer
- Marlex Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA207121
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (10135-812-01)
1000 TABLET, FILM COATED in 1 BOTTLE (10135-812-10)