Class II · Moderate risk
Pantoprazole Sodium Delayed-Release Tablets
CGMP deviations: tablets cracking
National Drug Code
Is NDC 13668-0096-90 recalled?
Pantoprazole Sodium · 90 TABLET, DELAYED RELEASE in 1 BOTTLE (13668-096-90)
Yes — this exact package was recalled
2 FDA recalls name the code 13668-0096-90 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 20 mg/1
- Form
- Tablet, Delayed Release · Oral
- Labeler
- Torrent Pharmaceuticals Limited
- Type
- Human Prescription Drug
- Product code
- 13668-0096
Recalls naming this package
Class II · Moderate risk
Pantoprazole Sodium Dr
Labeling: Label Mixup; PANTOPRAZOLE SODIUM DR, Tablet, 20 mg may be potentially mislabel as NORTRIPTYLINE HCL, Capsule, 75 mg, NDC 00093081301, Pedigree: W003694, EXP: 6/26/2014.
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
- 13668-0113 See recall 4
- 13668-0115 See recall 4
- 13668-0116 See recall 4
- 13668-0409 See recall 4
- 13668-0117 See recall 3
- 13668-0118 See recall 3
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