NDC 51662-1317
6% Hetastarch In 0.9% Sodium Chloride 6 g per 100 mL injection, 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 0409-7248.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that tests it). 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 Hospira, Inc. names for other drugs.
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Hetastarch: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 6 g per 100 mL
- Approval
- ANDA BA740193
- On the market since
- Nov 26, 2018
- Package NDCs
51662-1317-151662-1317-251662-1317-3- Official label
- DailyMed (National Library of Medicine), updated Jan 29, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?