NDC 51662-1457
Diltiazem Hci 100 mg injection, powder, lyophilized, for solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-4350.
Where the pills inside were 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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
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
- Dec 15, 2019
- Package NDCs
51662-1457-151662-1457-251662-1457-3- Official label
- DailyMed (National Library of Medicine), updated Mar 8, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?