Hydroxyzine Hydrochloride 70518-4170
Product NDC
70518-4170- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 28, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA217652
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(6)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-0)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-1)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-2)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-3)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-4)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-5)