NDC 21695-820
FEXOFENADINE HYDROCHLORIDE and PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg / 120 mg tablet, film coated, extended release
On the label: Rebel Distributors Corp... It's repackaged from NDC 0955-1705, made by Winthrop U.S. (FEXOFENADINE HYDROCHLORIDE and PSEUDOEPHEDRINE 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 Rebel Distributors Corp.. names for other drugs.
Product details
- Generic drug
- Fexofenadine and Pseudoephedrine: every company that makes it
- Form
- tablet, film coated, extended release
- Strength
- 60 mg / 120 mg
- Approval
- NDA NDA020786
- On the market since
- Nov 2, 2009
- Package NDCs
21695-820-14- Official label
- DailyMed (National Library of Medicine), updated Apr 13, 2011
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