Hydroxyzine Hydrochloride 71335-2185
Product NDC
71335-2185- Manufacturer
- Bryant Ranch Prepack
- 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 | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(5)
120 TABLET, FILM COATED in 1 BOTTLE (71335-2185-1)
20 TABLET, FILM COATED in 1 BOTTLE (71335-2185-2)
30 TABLET, FILM COATED in 1 BOTTLE (71335-2185-3)
60 TABLET, FILM COATED in 1 BOTTLE (71335-2185-4)
90 TABLET, FILM COATED in 1 BOTTLE (71335-2185-5)