NDC 67046-250
Guaifenesin 200 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged from NDC 0603-4886, made by Qualitest Pharmaceuticals (Organ-I Nr). 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 Coupler Enterprises Inc. names for other drugs.
Product details
- Generic drug
- Guaifenesin: every company that makes it
- Form
- tablet
- Strength
- 200 mg
- Approval
- Unapproved drug other
- On the market since
- Oct 6, 2010
- Package NDCs
67046-250-30- Official label
- DailyMed (National Library of Medicine), updated Oct 6, 2010
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?