NDC 70518-3783
Atorvastatin calcium 20 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Pharmaceutical Associates, Inc.'s NDC 75834-256.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Umedica Laboratories Private Limited | Vapi, India | Makes it and tests it | Problems found, fixed voluntarilyMar 29, 2024 · 4 inspections |
Product details
- Generic drug
- Atorvastatin: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA213853
- On the market since
- Jul 11, 2023
- Package NDCs
70518-3783-070518-3783-170518-3783-270518-3783-3- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2026
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