NDC 43353-244
Fexofenadine Hydrochloride 180 mg tablet, film coated
On the label: Aphena Pharma Solutions - Tennessee, Inc.. It's repackaged from NDC 0093-7253, made by Teva Pharmaceuticals USA Inc (Fexofenadine Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Aphena Pharma Solutions - Tennessee, Inc. names for other drugs.
Product details
- Generic drug
- Fexofenadine: every company that makes it
- Form
- tablet, film coated
- Strength
- 180 mg
- Approval
- ANDA ANDA076447
- On the market since
- Jul 1, 2010
- Package NDCs
43353-244-30- Official label
- DailyMed (National Library of Medicine), updated Jul 16, 2012
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?