NDC 68180-460
Minocycline Hydrochloride 55 mg tablet, extended release
On the label: Lupin Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Lupin Limited | Salcette, India | Makes it and packages it | Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Minocycline: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 55 mg
- Approval
- ANDA ANDA091424
- On the market since
- Feb 22, 2019
- Package NDCs
68180-460-0168180-460-06- Official label
- DailyMed (National Library of Medicine), updated Oct 30, 2023
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