Hydroxyzine Hydrochloride 71205-0083
Product NDC
71205-0083- Manufacturer
- Proficient Rx Lp
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 22, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA088619
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydroxyzine Dihydrochloride | 50 mg/1 |
Drug Class
Antihistamine [EPC]Histamine Receptor Antagonists [MoA]
Packaging Options(5)
15 TABLET, FILM COATED in 1 BOTTLE (71205-083-15)
20 TABLET, FILM COATED in 1 BOTTLE (71205-083-20)
30 TABLET, FILM COATED in 1 BOTTLE (71205-083-30)
60 TABLET, FILM COATED in 1 BOTTLE (71205-083-60)
90 TABLET, FILM COATED in 1 BOTTLE (71205-083-90)