NDC 50228-500
Diltiazem Hydrochloride 420 mg tablet, extended release
On the label: ScieGen Pharmaceuticals, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ScieGen Pharmaceuticals, INC. | Hauppauge, NY, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyMay 15, 2026 · 15 inspections, 1 with FDA action |
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 420 mg
- Approval
- ANDA ANDA216327
- On the market since
- Apr 6, 2023
- Package NDCs
50228-500-0550228-500-30- Official label
- DailyMed (National Library of Medicine), updated Oct 16, 2025
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