Drug
Who makes dextrose monohydrate, sodium chloride, and potassium chloride?
2 companies list dextrose monohydrate, sodium chloride, and potassium chloride as a human prescription drug. Forms: injection, solution. Routes: intravenous.
Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology
Companies listing dextrose monohydrate, sodium chloride, and potassium chloride
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Fresenius Kabi USA, LLCUnited States | injection, solution | ANDAANDA212348, ANDA213445, ANDA213523 | 9 | 6 |
| ICU Medical, Inc. | injection, solution | NDANDA018362, NDA018365, NDA019691 | 7 | 0 |
Enquiry
Common questions
- Who makes dextrose monohydrate, sodium chloride, and potassium chloride?
- 2 companies list dextrose monohydrate, sodium chloride, and potassium chloride as a human prescription drug in the openFDA NDC Directory, led by Fresenius Kabi USA, LLC, ICU Medical, Inc.. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
- Is there a generic dextrose monohydrate, sodium chloride, and potassium chloride?
- 1 company lists dextrose monohydrate, sodium chloride, and potassium chloride under an abbreviated new drug application (ANDA), the application type used for generics, and 1 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.