Amlodipine 1 mg/mL oral suspension
Ingredients
| Ingredient | Role | For 100 mL |
|---|---|---|
| Amlodipine (as besylate) | active | 100 mg |
| Syrup and suspending vehicle, 1:1 (v/v) | vehicle | q.s. to 100 mL |
- Strength
- 1 mg/mL
- Starting material
- Amlodipine 5 mg or 10 mg tablets, or capsules
- Container
- See the study
Amounts are ClinDose's arithmetic from the study's concentration; follow the study for the method.
Storage and beyond-use date
| Storage | BUD | Basis |
|---|---|---|
| Refrigerated | 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
Elzayat E, Alotaibi HF, Al-Agamy MH, Alharabi LA, Alhuzani MR. Engineering stable Amlodipine suspensions for flexible compounding at King Khaled University Hospital. Saudi Pharm J. 2025;33(4):23. PMID 40627275. PMC12238434. License: CC BY-NC-ND (checked 2026-11-06). Read the article · DOI
For licensed clinicians. Use with clinical judgment.