NDC 53808-0863
Gemfibrozil 600 mg tablet, film coated
On the label: State of Florida DOH Central Pharmacy. It's repackaged: State of Florida DOH Central Pharmacy rebottles it from PuraCap Laboratories LLC dba Blu Pharmaceuticals's NDC 24658-260.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Caribe Holdings (Cayman) Co. Ltd. DBA PuraCap Caribe | Location not on file | Makes it | Not inspected on record |
Repackaging site
- State of Florida DOH Central Pharmacy, Location not on file · repackages it
Product details
- Generic drug
- Gemfibrozil: every company that makes it
- Form
- tablet, film coated
- Strength
- 600 mg
- Approval
- ANDA ANDA078012
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0863-1- Official label
- DailyMed (National Library of Medicine), updated Sep 11, 2013
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