NDC 0591-2132
Doxylamine succinate and pyridoxine hydrochloride 10 mg tablet, delayed release
On the label: Actavis Pharma, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Actavis Pharma, Inc. names for other drugs.
Recalls
- Jan 18, 2022 · Class II · Teva Pharmaceuticals USA
Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient
Lots: Lot# 100025842, 100028023, Exp Date 08/2023
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Doxylamine and Pyridoxine: every company that makes it
- Form
- tablet, delayed release, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA205811
- On the market since
- Jun 21, 2019
- Package NDCs
0591-2132-01- Official label
- DailyMed (National Library of Medicine), updated Sep 1, 2025
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