NDC 17856-0092
Oxybutynin Chloride 5 mg per 5 mL syrup
On the label: Atlantic Biologicals Corps.. It's repackaged from NDC 60432-092, made by Morton Grove Pharmaceuticals, Inc. (Oxybutynin Chloride). 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 and relabels 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 Atlantic Biologicals Corps. names for other drugs.
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- syrup
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA074868
- On the market since
- Feb 12, 1997
- Package NDCs
17856-0092-1- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2021
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