NDC 60687-309
Linezolid 600 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Camber Pharmaceuticals Inc.'s NDC 31722-749.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hetero Labs Limited | Mahabubnagar, India | Makes it | Problems found, fixed voluntarilyAug 12, 2022 · 5 inspections, 1 with FDA action |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Linezolid: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 600 mg
- Approval
- ANDA ANDA204239
- On the market since
- Feb 15, 2018
- Package NDCs
60687-309-1160687-309-21- Official label
- DailyMed (National Library of Medicine), updated Nov 22, 2024
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