Class II ยท Moderate risk
Tizanidine Tablets
Failed Dissolution Specifications: this repackaged product was recalled by the manufacturer, Dr. Reddy's Laboratories, Inc., due to out of specification results for dissolution.
National Drug Code
Is NDC 68084-0645-01 recalled?
Tizanidine · 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-645-01) / 1 TABLET in 1 BLISTER PACK (68084-645-11)
Yes — this exact package was recalled
1 FDA recall names the code 68084-0645-01 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
- Tizanidine
- Strength
- TIZANIDINE HYDROCHLORIDE 4 mg/1
- Form
- Tablet · Oral
- Labeler
- American Health Packaging
- Type
- Human Prescription Drug
- Product code
- 68084-0645
Recalls naming this package
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
- 68084-0295 See recall 3
- 68084-0446 See recall 3
- 68084-0214 Benzonatate 2
- 68084-0279 See recall 2
- 68084-0325 See recall 2
- 68084-0390 See recall 2
Free recall alerts
Know the day your medication is recalled
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