NDC 17856-0149
Oxybutynin Chloride 5 mg per 5 mL syrup
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Lannett Company, Inc.'s NDC 54838-510.
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 Lannett Company, Inc. names for other drugs.
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- syrup, oral
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA074520
- On the market since
- Mar 29, 1996
- Package NDCs
17856-0149-1- Official label
- DailyMed (National Library of Medicine), updated Jul 9, 2026
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