Hydroxyzine Hydrochloride 16571-0114
Product NDC
16571-0114- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 22, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA217652
Need to source Hydroxyzine Hydrochloride? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (16571-114-01)
1000 TABLET, FILM COATED in 1 BOTTLE (16571-114-10)
500 TABLET, FILM COATED in 1 BOTTLE (16571-114-50)