Furosemide 2 mg/mL oral solution
Ingredients
| Ingredient | Role | For 100 mL |
|---|---|---|
| Furosemide | active | 200 mg |
| Ethanol-free aqueous vehicle with sorbitol (see the study) | vehicle | q.s. to 100 mL |
- Strength
- 2 mg/mL
- Starting material
- Furosemide bulk powder
- Container
- Brown glass bottles with polypropylene screw caps
Amounts are ClinDose's arithmetic from the study's concentration; follow the study for the method.
Storage and beyond-use date
| Storage | BUD | Basis |
|---|---|---|
| Room temperature | 90 days | Cited stability study. Duration supported by the cited stability study for this formula, container, and storage. |
Only the storage conditions the source covers are listed. Use the BUD assistant for other cases. The BUD may not be later than any component's expiration date. Verify against the current official USP chapter.
Ingredient checks
No FDA compounding list or NIOSH flags for the active ingredient.
Source
Sombié CB, Guetambaba JEK, Diawara HZ, et al.. Hospital preparations of ethanol-free furosemide oral solutions: Formulation and stability study. J Adv Pharm Technol Res. 2022;13(2):128-132. PMID 35464657. PMC9022368. License: CC BY-NC-SA (checked 2026-11-06). Read the article · DOI
For licensed clinicians. Use with clinical judgment.