NDC 0409-4350
Diltiazem Hydrochloride 100 mg injection, powder, lyophilized, for solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Product details
- Generic drug
- Diltiazem: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 100 mg
- Approval
- ANDA ANDA075853
- On the market since
- Apr 30, 2005
- Package NDCs
0409-4350-030409-4350-13- Official label
- DailyMed (National Library of Medicine), updated May 24, 2026
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