Cetirizine Hydrochloride 68016-0939
Product NDC
68016-0939- Manufacturer
- Chain Drug Consortium, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- December 27, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077498
Active Ingredients
| Ingredient | Strength |
|---|---|
| Cetirizine Hydrochloride | 10 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(4)
30 TABLET in 1 BOTTLE (68016-939-30)
14 TABLET in 1 BLISTER PACK (68016-939-54)
60 TABLET in 1 BOTTLE (68016-939-60)
90 TABLET in 1 BOTTLE (68016-939-90)