Class III · Low risk
Oxybutynin Chloride Extended-Release Tablets USP 10 mg
Failed Dissolution Specifications
National Drug Code
Is NDC 42291-0634-01 recalled?
Oxybutynin Chloride Extended Release · 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-634-01)
Yes — this exact package was recalled
1 FDA recall names the code 42291-0634-01 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
- Oxybutynin Chloride
- Strength
- OXYBUTYNIN CHLORIDE 10 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- AvKARE
- Type
- Human Prescription Drug
- Product code
- 42291-0634
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
- 42291-0297 See recall 1
- 42291-0367 Lamotrigine 1
- 42291-0368 Lamotrigine 1
- 42291-0459 See recall 1
- 42291-0460 See recall 1
- 42291-0461 See recall 1
Free recall alerts
Know the day your medication is recalled
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