Fexofenadine Hydrochloride 68016-0995
Product NDC
68016-0995- Manufacturer
- Chain Drug Consortium, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- April 1, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA076502
Active Ingredients
| Ingredient | Strength |
|---|---|
| Fexofenadine Hydrochloride | 180 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(2)
1 BOTTLE in 1 CARTON (68016-995-03) / 30 TABLET in 1 BOTTLE
1 BOTTLE in 1 CARTON (68016-995-45) / 45 TABLET in 1 BOTTLE