Class II · Moderate risk
Pantoprazole Sodium
Discoloration: Firm received five (5) complaints stating that, "Tablets discolored darker than normal and have lighter-colored spots."
National Drug Code
Is NDC 31722-0713-10 recalled?
Pantoprazole Sodium · 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-10)
Yes — this exact package was recalled
2 FDA recalls name the code 31722-0713-10 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.
2 of these recalls are still ongoing.
- Active ingredient
- Pantoprazole
- Strength
- PANTOPRAZOLE SODIUM 40 mg/1
- Form
- Tablet, Delayed Release · Oral
- Labeler
- Camber Pharmaceuticals, Inc.
- Type
- Human Prescription Drug
- Product code
- 31722-0713
Recalls naming this package
Class II · Moderate risk
Pantoprazole Sodium Delayed Release Tablets USP 40mg
CGMP Deviations: Discoloration
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
- 31722-0726 Montelukast Sodium 3
- 31722-0270 See recall 1
- 31722-0307 Ketorolac Tromethamine 1
- 31722-0513 Simvastatin 1
- 31722-0525 Finasteride 1
- 31722-0530 Torsemide 1
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