Quick answers
- What is Md Gastroview?
- Md Gastroview is a brand name of Diatrizoate meglumine and diatrizoate sodium, a prescription medicine. The FDA NDC Directory lists 1 Md Gastroview product in 1 strength and form.
- Who makes Md Gastroview?
- Liebel-Flarsheim holds the FDA application for Md Gastroview (ANDA087388, approved September 2, 1981).
- Is there a generic or store brand of Md Gastroview?
- Other products of Diatrizoate meglumine and diatrizoate sodium are listed with the FDA, but none in exactly the same strength and form as a Md Gastroview product.
- Has Md Gastroview been recalled?
- FDA enforcement reports list 1 recall of Md Gastroview products; the newest started May 15, 2015. A recall usually concerns specific lots, not every product.
What Md Gastroview is
Each Md Gastroview product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Diatrizoate meglumine and diatrizoate sodium · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| diatrizoate meglumine 600 mg/mL · diatrizoate sodium 100 mg/mL solution (oral, rectal) | Md Gastroview | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Diatrizoate meglumine and diatrizoate sodium →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA087388 | Liebel-Flarsheim | September 2, 1981 | 1 |
Companies that list Md Gastroview
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Md Gastroview products.
- Liebel-Flarsheim Company LLC1 product
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
May 15, 2015 · Class II · Terminated · D-1132-2015
Labeling: incorrect or missing lot number and/or expiration date
MD-Gastroview (Diatrizoate Meglumine and Diatrizoate Sodium Solution USP); 37% Organically Bound Iodine For Gastrointestinal Radiography; Oral or rectal use only; Rx only; 30 mL; Single-Unit Container; ; Mallinckrodt Inc — Mallinckrodt, Inc.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.