NDC 49999-772
Fexofenadine Hydrochloride 180 mg tablet, film coated
On the label: Lake Erie Medical DBA Quality Care Products LLC. It's repackaged from NDC 66993-109, made by Prasco Laboratories (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. 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 Lake Erie Medical DBA Quality Care Products LLC names for other drugs.
Product details
- Generic drug
- Fexofenadine: every company that makes it
- Form
- tablet, film coated
- Strength
- 180 mg
- Approval
- ANDA ANDA020872
- On the market since
- Jun 7, 2010
- Package NDCs
49999-772-30- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2010
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