NDC 68382-091
Benzonatate 200 mg capsule, liquid filled
On the label: Zydus Pharmaceuticals (USA) Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Zydus Lifesciences Limited | Ahmedabad, India | Makes it and tests it | Problems found, fixed voluntarilyAug 5, 2022 · 10 inspections, 3 with FDA action |
Recalls
- Dec 23, 2014 · Class II · Zydus Pharmaceuticals USA Inc
Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.
Lots: Lot #: MP2625, MP2626, MP2627 Exp 2/16; MP4875, MP4876, MP4877, MP4878 Exp 4/16; MP6482, MP6483, MP6484, MP6493, MP6494 Exp 6/16
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Benzonatate: every company that makes it
- Form
- capsule, liquid filled, oral
- Strength
- 200 mg
- Approval
- ANDA ANDA040597
- On the market since
- Apr 9, 2007
- Package NDCs
68382-091-01- Official label
- DailyMed (National Library of Medicine), updated Mar 23, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?