NDC 70518-4652
Metformin hydrochloride 1000 mg tablet, extended release
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ajanta Pharma USA Inc.'s NDC 27241-189.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ajanta Pharma Limited | Chhatrapati Sambhajinagar, India | Makes it | Problems found, fixed voluntarilyApr 21, 2026 · 6 inspections |
Product details
- Generic drug
- Metformin: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 1000 mg
- Approval
- ANDA ANDA213651
- On the market since
- May 4, 2026
- Package NDCs
70518-4652-070518-4652-1- Official label
- DailyMed (National Library of Medicine), updated Sep 21, 2026
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