Gabapentin 100 mg/mL oral suspension
Ingredients
| Ingredient | Role | For 100 mL |
|---|---|---|
| Gabapentin | active | 10 g |
| Oral Mix or Oral Mix SF suspending vehicle | vehicle | q.s. to 100 mL |
- Strength
- 100 mg/mL
- Starting material
- Bulk powder or capsule contents
- Container
- Amber plastic bottles and amber plastic oral syringes
- Crystallization occurred at 5 °C: do not refrigerate.
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
Friciu M, Roullin VG, Leclair G. Stability of gabapentin in extemporaneously compounded oral suspensions. PLoS One. 2017;12(4):e0175208. PMID 28414771. PMC5393583. License: CC BY (checked 2026-11-06). Read the article · DOI
For licensed clinicians. Use with clinical judgment.