Class II · Moderate risk
Tizanidine Tablets
Presence of Foreign tablets/capsules - identified as tizanidine 2 mg tablets.
National Drug Code
Is NDC 55111-0180-10 recalled?
Tizanidine · 1000 TABLET in 1 BOTTLE (55111-180-10)
Yes — this exact package was recalled
1 FDA recall names the code 55111-0180-10 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.
1 of these recalls is still ongoing.
- Active ingredient
- Tizanidine
- Strength
- TIZANIDINE HYDROCHLORIDE 4 mg/1
- Form
- Tablet · Oral
- Labeler
- Dr. Reddy's Laboratories Limited
- Type
- Human Prescription Drug
- Product code
- 55111-0180
Recalls naming this package
Class II · Moderate risk
Tizanidine Tablets USP
Failed dissolution specification: Out of specification results observed in 24-month long term stability testing.
Class II · Moderate risk
Tizanidine HCl Tablets
Failed Tablet/Capsule Specification: Some tablets are shaved
Class III · Low risk
Tizanidine Tablets USP
Labeling Illegible: There is a possibility that the bottle labels do not contain the strength of the product as well as other printing details.
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
- 55111-0121 Atorvastatin Calcium 4
- 55111-0123 Atorvastatin Calcium 4
- 55111-0136 Zenatane 3
- 55111-0179 Tizanidine 3
- 55111-0320 Glimepiride 3
- 55111-0533 Divalproex Sodium 3
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