NDC 42708-082
Benzonatate 200 mg capsule
On the label: QPharma, Inc.. It's repackaged: QPharma, Inc. rebottles it from Ascend Laboratories, LLC's NDC 67877-575.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Softgel Healthcare Private Limited | Chengalpattu, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyFeb 14, 2025 · 4 inspections |
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Benzonatate: every company that makes it
- Form
- capsule, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA040627
- On the market since
- Mar 22, 2017
- Package NDCs
42708-082-21- Official label
- DailyMed (National Library of Medicine), updated Dec 21, 2025
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