Class II · Moderate risk
Pantoprazole Sodium Delayed-Release Tablets
CGMP Deviations: Presence of dark brown discoloration on edges of tablets
National Drug Code
Is NDC 59746-0284-90 recalled?
Pantoprazole Sodium
Yes — this exact package was recalled
5 FDA recalls name the code 59746-0284-90 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
- Pantoprazole Sodium
- Strength
- PANTOPRAZOLE SODIUM 40 mg/1
- Form
- Tablet, Delayed Release
- Labeler
- Jubilant Cadista Pharmaceuticals INC.
- Type
- Drug for Further Processing
- Product code
- 59746-0284
Recalls naming this package
Class II · Moderate risk
Pantoprazole Sodium Delayed Release Tablets
CGMP Deviation: Presence of dark brown discoloration on edges of tablets.
Class II · Moderate risk
Pantoprazole Sodium Delayed-Release Tablets
Discoloration: Expansion of an earlier recall due to the presence of dark brown discoloration on the edges of the tablets.
Class II · Moderate risk
Pantoprazole Sodium Delayed-Release Tablets
Discoloration: Presence of dark discoloration or brown spots on the edges of the tablets.
Class II · Moderate risk
Pantoprazole Sodium Delayed Release Tablets USP
cGMP Deviations: Oral products were not manufactured in accordance with Good Manufacturing Practices.
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
- 59746-0001 See recall 5
- 59746-0122 Meclizine Hydrochloride 2
- 59746-0360 valsartan 2
- 59746-0363 See recall 2
- 59746-0003 See recall 1
- 59746-0113 Prochlorperazine Maleate 1
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