Hydroxyzine Hydrochloride 59651-0500
Product NDC
59651-0500- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 7, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA087871
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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 (59651-500-01)
500 TABLET, FILM COATED in 1 BOTTLE (59651-500-05)
1000 TABLET, FILM COATED in 1 BOTTLE (59651-500-99)