Hydroxyzine Hydrochloride 71610-0735
Product NDC
71610-0735- Manufacturer
- Aphena Pharma Solutions - Tennessee, Llc
- 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(5)
30 TABLET, FILM COATED in 1 BOTTLE (71610-735-30)
60 TABLET, FILM COATED in 1 BOTTLE (71610-735-53)
90 TABLET, FILM COATED in 1 BOTTLE (71610-735-60)
120 TABLET, FILM COATED in 1 BOTTLE (71610-735-70)
180 TABLET, FILM COATED in 1 BOTTLE (71610-735-80)