NDC 51662-1520
0.9% Sodium Chloride 900 mg 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 ICU Medical Inc.'s NDC 0990-7984.
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 ICU Medical Inc. names for other drugs.
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Oct 27, 2025 · Class II · Otsuka ICU Medical LLC
Lack of Assurance of Sterility: Potential for flexible container leaks.
Lots: Lot # 1029921, Exp Date: 28 February 2027 - Nov 9, 2022 · Class II · ICU Medical Inc
Lack of assurance of sterility: Bags have the potential to leak in the flexible containers which may compromise sterility.
Lots: Lot: 5829936, Exp. MAR 31 2024
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sodium Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 900 mg per 100 mL
- Approval
- NDA NDA016366
- On the market since
- May 21, 2020
- Package NDCs
51662-1520-1- Official label
- DailyMed (National Library of Medicine), updated May 21, 2020
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?