Class II · Moderate risk
MD-Gastroview
Labeling: incorrect or missing lot number and/or expiration date
National Drug Code
Is NDC 0019-4816-04 recalled?
Md Gastroview · 25 BOTTLE, GLASS in 1 BOX (0019-4816-04) / 30 mL in 1 BOTTLE, GLASS
Yes — this exact package was recalled
1 FDA recall names the code 0019-4816-04 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- diatrizoate meglumine and diatrizoate sodium
- Strength
- DIATRIZOATE MEGLUMINE 600 mg/mL; DIATRIZOATE SODIUM 100…
- Form
- Solution · Oral, Rectal
- Labeler
- Liebel-Flarsheim Company LLC
- Type
- Human Prescription Drug
- Product code
- 0019-4816
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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