Hydroxyzine Hydrochloride 72162-1333
Product NDC
72162-1333- 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
- ANDA040602
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(7)
20 TABLET, FILM COATED in 1 BOTTLE (72162-1333-2)
30 TABLET, FILM COATED in 1 BOTTLE (72162-1333-3)
15 TABLET, FILM COATED in 1 BOTTLE (72162-1333-4)
500 TABLET, FILM COATED in 1 BOTTLE (72162-1333-5)
60 TABLET, FILM COATED in 1 BOTTLE (72162-1333-6)
10 TABLET, FILM COATED in 1 BOTTLE (72162-1333-8)
90 TABLET, FILM COATED in 1 BOTTLE (72162-1333-9)