NDC 51662-1567
Cosyntropin 0.25 mg per 1 mL 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 Sandoz Inc.'s NDC 0781-3440.
Where the pills inside were made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Sandoz Inc. names for other drugs.
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Cosyntropin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 0.25 mg per 1 mL
- Approval
- ANDA ANDA202147
- On the market since
- Jul 10, 2021
- Package NDCs
51662-1567-1- Official label
- DailyMed (National Library of Medicine), updated Feb 22, 2024
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