NDC 51662-1635
THIAMINE HYDROCHLORIDE injection, solution 100 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Dr. Reddy's Laboratories Inc.'s NDC 43598-050.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Dr.reddy's Laboratories Limited | Visakhapatnam, India | Makes it and tests it | Problems found, fixed voluntarilyMay 17, 2024 · 9 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Thiamine Ion: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 100 mg per 1 mL
- Approval
- ANDA ANDA080571
- On the market since
- Sep 26, 2023
- Package NDCs
51662-1635-151662-1635-251662-1635-3- Official label
- DailyMed (National Library of Medicine), updated May 7, 2026
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