Cetirizine Hydrochloride 00378-3635
Product NDC
00378-3635- Manufacturer
- Mylan Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 27, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA076677
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 5 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3635-01)