Hydroxyzine Hydrochloride 71335-3035
Product NDC
71335-3035- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 7, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA087871
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
1000 TABLET, FILM COATED in 1 BOTTLE (71335-3035-1)