Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Cimbar Performance Minerals, Inc. | Chatsworth, GA, United States | Makes the active ingredient | Problems found, fixed voluntarilyJul 18, 2025 · 4 inspections |
| E-Z-EM Canada Inc | Anjou, Canada | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 20, 2023 · 4 inspections |
Recalls
- Apr 13, 2022 · Class II · Mckesson Medical-Surgical Inc. Corporate Office
cGMP deviations: Temperature abuse
Lots: McKesson Medical-Surgical (MMS) is not able to identify the particular lot number received by a particular consignee for the recalled prescription products. Each letter includes the date it was distributed to customers and the dates that impacted product may have been shipped to the customer. - Jul 2, 2014 · Class III · Bracco Diagnostic Inc
Subpotent Drug: Low out of specification results for both pH and assay obtained during routine stability testing after 36 months.
Lots: Lot #'s: 64205, 64206, 64200, 64201, 64202, 64203, 64204, 64207, 64264, Exp 05/15; 64265, 64267, 64268, 64270, 64271, Exp 06/15
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Barium: every company that makes it
- Form
- powder, for suspension, oral
- Strength
- 980 mg per 1 g
- Approval
- NDA NDA208036
- On the market since
- Jan 11, 2016
- Package NDCs
32909-764-01- Official label
- DailyMed (National Library of Medicine), updated Apr 15, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?