NDC 42291-618
Minoxidil 2.5 mg tablet
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Caraco Pharmaceutical Laboratories, Ltd.'s NDC 53489-386.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Frontida BioPharm, LLC | Philadelphia, PA, United States | Makes it | No problems foundApr 2, 2026 · 10 inspections, 1 with FDA action |
Product details
- Generic drug
- Minoxidil: every company that makes it
- Form
- tablet, oral
- Strength
- 2.5 mg
- Approval
- ANDA ANDA072708
- On the market since
- Aug 1, 2013
- Package NDCs
42291-618-0142291-618-90- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2026
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