Hydroxyzine Hydrochloride 70518-1265
Product NDC
70518-1265- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 19, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA204279
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
60 TABLET in 1 BOTTLE, PLASTIC (70518-1265-1)
100 POUCH in 1 BOX (70518-1265-2) / 1 TABLET in 1 POUCH (70518-1265-3)
100 POUCH in 1 BOX (70518-1265-4) / 1 TABLET in 1 POUCH (70518-1265-5)