Hydroxyzine Hydrochloride 68999-0050
Product NDC
68999-0050- Manufacturer
- Chartwell Governmental & Specialty Rx, Llc.
- Dosage Form
- Syrup
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 12, 1982
- Listing Expires
- December 31, 2026
- Application
- ANDA087294
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/25mL |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
2 TRAY in 1 BOX (68999-050-24) / 10 CUP in 1 TRAY / 25 mL in 1 CUP (68999-050-52)