Drug
Who makes dextrose monohydrate and sodium chloride?
3 companies list dextrose monohydrate and sodium 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 and sodium chloride
| Company | Forms | Application | NDCs | Registered sites |
|---|---|---|---|---|
| Fresenius Kabi USA, LLCUnited States | injection, solution | ANDAANDA211194, ANDA211211, ANDA211221 | 4 | 6 |
| ICU Medical, Inc. | injection, solution | NDANDA017585, NDA017606, NDA017607 | 4 | 0 |
| Becton Dickinson and CompanyUnited States | injection, solution | ANDAANDA211211, ANDA211276 | 2 | 2 |
Enquiry
Common questions
- Who makes dextrose monohydrate and sodium chloride?
- 3 companies list dextrose monohydrate and sodium chloride as a human prescription drug in the openFDA NDC Directory, led by Fresenius Kabi USA, LLC, ICU Medical, Inc., Becton Dickinson and Company. 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 and sodium chloride?
- 2 companies list dextrose monohydrate and sodium 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.