Cetirizine Hydrochloride 47335-0344
Product NDC
47335-0344- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Chewable
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- September 9, 2011
- Listing Expires
- December 31, 2027
- Application
- ANDA090142
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(2)
30 TABLET, CHEWABLE in 1 BOTTLE (47335-344-83)
100 TABLET, CHEWABLE in 1 BOTTLE (47335-344-88)