Hydroxyzine Hydrochloride 62135-0750
Product NDC
62135-0750- Manufacturer
- Chartwell 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 | 10 mg/5mL |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
473 mL in 1 BOTTLE (62135-750-47)