NDC 42708-183
Hyoscyamine Sulfate TAB 0.125 mg tablet
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Acella Pharmaceuticals, LLC's NDC 42192-340.
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 Acella Pharmaceuticals, LLC names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Hyoscyamine: every company that makes it
- Form
- tablet, oral
- Strength
- 0.125 mg
- Approval
- unapproved drug other
- On the market since
- May 19, 2011
- Package NDCs
42708-183-56- Official label
- DailyMed (National Library of Medicine), updated Dec 16, 2025
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