Hydroxyzine Hydrochloride 62135-0546
Product NDC
62135-0546- Manufacturer
- Chartwell Rx, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 30, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA040804
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(2)
500 TABLET, FILM COATED in 1 BOTTLE (62135-546-05)
120 TABLET, FILM COATED in 1 BOTTLE (62135-546-12)