Hydroxyzine Hydrochloride 51655-0589
Product NDC
51655-0589- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 8, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA088618
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 25 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(3)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-25)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-52)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-589-53)