Class II · Moderate risk
Gastrografin
cGMP deviations: Temperature abuse
National Drug Code
Is NDC 0270-0445-35 recalled?
Gastrografin · 24 BOTTLE in 1 BOX (0270-0445-35) / 30 mL in 1 BOTTLE
Yes — this exact package was recalled
1 FDA recall names the code 0270-0445-35 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 660 mg/mL; DIATRIZOATE SODIUM 100…
- Form
- Liquid · Oral, Rectal
- Labeler
- Bracco Diagnostics Inc
- Type
- Human Prescription Drug
- Product code
- 0270-0445
Recalls naming this package
Class II · Moderate risk
Gastrografin
Presence of foreign substance: One lot of the product may contain black foreign particles
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
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.