NDC 68084-059
Zafirlukast 20 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Dr.Reddy's Laboratories Ltd.'s NDC 55111-626.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr. Reddy's Laboratories Limited | Medchal-Malkajgiri, India | Makes it and tests it | Problems found, fixed voluntarilyOct 27, 2023 · 8 inspections |
Repackaging site
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Zafirlukast: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA090372
- On the market since
- Jun 3, 2013
- Package NDCs
68084-059-1168084-059-21- Official label
- DailyMed (National Library of Medicine), updated Oct 11, 2024
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