Hydroxyzine Hydrochloride 72789-0269
Product NDC
72789-0269- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- 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(1)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-269-30)