NDC 70518-1336
Minocycline Hydrochloride 100 mg capsule
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-211.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Aurobindo Pharma Limited | Medchal, India | Makes it and tests it | Problems found, fixed voluntarilyJul 21, 2023 · 13 inspections, 1 with FDA action |
Product details
- Generic drug
- Minocycline: every company that makes it
- Form
- capsule, oral
- Strength
- 100 mg
- Approval
- ANDA ANDA065470
- On the market since
- Aug 1, 2018
- Package NDCs
70518-1336-070518-1336-170518-1336-270518-1336-3- Official label
- DailyMed (National Library of Medicine), updated Jul 3, 2026
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