NDC 65862-883
Minocycline Hydrochloride 55 mg tablet, film coated, extended release
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Mahabubnagar, India | Makes it and tests it | Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Minocycline: every company that makes it
- Form
- tablet, film coated, extended release, oral
- Strength
- 55 mg
- Approval
- ANDA ANDA202261
- On the market since
- Aug 21, 2019
- Package NDCs
65862-883-0165862-883-0565862-883-3065862-883-99- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2025
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