NDC 23155-913
Oxybutynin Chloride 5 mg tablet
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc. | East Brunswick, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
Product details
- Generic drug
- Oxybutynin: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA211682
- On the market since
- Jun 1, 2026
- Package NDCs
23155-913-0123155-913-0523155-913-10- Official label
- DailyMed (National Library of Medicine), updated May 20, 2026
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