Hydroxyzine Hydrochloride 70518-1692
Product NDC
70518-1692- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 26, 2018
- Listing Expires
- December 31, 2027
- Application
- ANDA204279
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(1)
30 TABLET in 1 BOTTLE, PLASTIC (70518-1692-2)