Levocetirizine Dihydrochloride 33342-0200
Product NDC
33342-0200- Manufacturer
- Macleods Pharmaceuticals Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 11, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA205564
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Levocetirizine Dihydrochloride | 5 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (33342-200-07)
90 TABLET, FILM COATED in 1 BOTTLE (33342-200-10)