Activated Charcoal Oral Suspension
Brand names: Actidose, Actidose Aqua
Category: Other
FDA status: To Be Discontinued · Last FDA update: May 15, 2026 · First posted: May 15, 2026 · 1 manufacturers, 5 listed presentations
As of May 15, 2026, the FDA lists Activated Charcoal Oral Suspension as being discontinued. Of 5 manufacturer presentations, 5 Not specified.
| Presentation & package NDC | Manufacturer | Availability | FDA note |
|---|---|---|---|
| Actidose, Oral Suspension, 208 mg/1 mL (NDC 0574-0520-76) NDC 0574-0520-76 |
Padagis US LLC | Not specified | Discontinuation of the manufacture of the drug |
| Actidose, Oral Suspension, 208 mg/1 mL (NDC 0574-0520-74) NDC 0574-0520-74 |
Padagis US LLC | Not specified | Discontinuation of the manufacture of the drug |
| Actidose Aqua, Oral Suspension, 208 mg/1 mL (NDC 0574-0521-74) NDC 0574-0521-74 |
Padagis US LLC | Not specified | Discontinuation of the manufacture of the drug |
| Actidose Aqua, Oral Suspension, 208 mg/1 mL (NDC 0574-0521-25) NDC 0574-0521-25 |
Padagis US LLC | Not specified | Discontinuation of the manufacture of the drug |
| Actidose Aqua, Oral Suspension, 208 mg/1 mL (NDC 0574-0521-76) NDC 0574-0521-76 |
Padagis US LLC | Not specified | Discontinuation of the manufacture of the drug |
Related medications in shortage
Other Other medications currently on the FDA shortage list — useful context if you and your prescriber are weighing alternatives. Always confirm with your pharmacist.
Change log
Tracking began Oct 1, 2026. We check the FDA every 6 hours; any real change - a manufacturer moving from Limited to Available, a new recovery date, a new listing - shows up here with its date.
Cite this: “FDA drug-shortage status for Activated Charcoal Oral Suspension (FDA data as of May 15, 2026). Shortage Watch, openFDA.”
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FDA data last synced Oct 1, 2026 (FDA record dated Sep 30, 2026).