NDC 12634-416
Furosemide 20 mg tablet
On the label: Apotheca, Inc.. It's repackaged: Apotheca, Inc. rebottles it from Excellium Pharmaceutical Inc.'s NDC 64125-116.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Excellium Pharmaceutical Inc. | Location not on file | Makes it | Not inspected on record |
Repackaging site
- Apotheca Inc., Phoenix, AZ, United States · repackages it and relabels it
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- tablet
- Strength
- 20 mg
- Approval
- ANDA ANDA077293
- On the market since
- Feb 24, 2016
- Package NDCs
12634-416-0012634-416-0112634-416-0912634-416-1212634-416-1812634-416-4012634-416-4212634-416-4512634-416-5012634-416-5212634-416-5412634-416-57- Official label
- DailyMed (National Library of Medicine), updated Jan 18, 2017
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