Hydroxyzine Hydrochloride 71335-0935
Product NDC
71335-0935- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 9, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA088618
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(8)
30 TABLET, FILM COATED in 1 BOTTLE (71335-0935-1)
60 TABLET, FILM COATED in 1 BOTTLE (71335-0935-2)
20 TABLET, FILM COATED in 1 BOTTLE (71335-0935-3)
100 TABLET, FILM COATED in 1 BOTTLE (71335-0935-4)
15 TABLET, FILM COATED in 1 BOTTLE (71335-0935-5)
90 TABLET, FILM COATED in 1 BOTTLE (71335-0935-6)
19 TABLET, FILM COATED in 1 BOTTLE (71335-0935-7)
10 TABLET, FILM COATED in 1 BOTTLE (71335-0935-8)