NDC 70518-4454
Propranolol Hydrochloride 20 mg tablet
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Ipca Laboratories Limited's NDC 83980-006.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Ipca Laboratories Limited | Silvassa, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 26, 2023 · 5 inspections, 2 with FDA action |
Product details
- Generic drug
- Propranolol: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA078955
- On the market since
- Aug 22, 2025
- Package NDCs
70518-4454-070518-4454-1- Official label
- DailyMed (National Library of Medicine), updated Mar 19, 2026
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