Class II · Moderate risk
Doxylamine Succinate and Pyridoxine Hydrochloride Delayed-Release Tablets 10 mg/10 mg
Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient
National Drug Code
Is NDC 0591-2132-01 recalled?
Doxylamine succinate and pyridoxine hydrochloride · 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0591-2132-01)
Yes — this exact package was recalled
1 FDA recall names the code 0591-2132-01 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
- Doxylamine succinate and pyridoxine hydrochloride
- Strength
- DOXYLAMINE SUCCINATE 10 mg/1; PYRIDOXINE HYDROCHLORIDE 10…
- Form
- Tablet, Delayed Release · Oral
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug
- Product code
- 0591-2132
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
Free recall alerts
Know the day your medication is recalled
Tell us what you take. When FDA posts a recall announcement or classifies a recall for one of your medications, we email you in plain English, with what to check. No account needed.