NDC 65862-557
Minocycline Hydrochloride 115 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
- 115 mg
- Approval
- ANDA ANDA202261
- On the market since
- Sep 28, 2018
- Package NDCs
65862-557-3065862-557-99- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?