NDC 51662-1308
0.9% Sodium Chloride 900 mg per 100 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged from NDC 0409-7983, made by Hospira, Inc. (Sodium Chloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that relabels 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 HF Acquisition Co. LLC. DBA HealthFirst names for other drugs.
Product details
- Generic drug
- Sodium Cation: every company that makes it
- Form
- injection, solution
- Strength
- 900 mg per 100 mL
- Approval
- NDA NDA016366
- On the market since
- Oct 18, 2018
- Package NDCs
51662-1308-1- Official label
- DailyMed (National Library of Medicine), updated Feb 21, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?