NDC 51662-1647
Cyanocobalamin 1000 ug 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 American Regent, Inc.'s NDC 0517-0031.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Shirley, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 24, 2024 · 12 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Jul 24, 2026 · Class II · American Regent, Inc.
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Lots: Lot #: 24297, Exp. Date 8/31/2026; 24364, Exp. Date: 10/31/2026; - Jul 24, 2026 · Class II · American Regent, Inc.
Presence of Particulate Matter: Product contaminated with particulate matter identified as hair, glass and/or paraformaldehyde
Lots: Lot #: 25082, Exp. Date: 3/31/2027.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Cyanocobalamin: every company that makes it
- Form
- injection, solution, intramuscular; subcutaneous
- Strength
- 1000 ug per 1 mL
- Approval
- ANDA ANDA080737
- On the market since
- Sep 30, 1990
- Package NDCs
51662-1647-251662-1647-3- Official label
- DailyMed (National Library of Medicine), updated Apr 10, 2024
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