NDC 0591-2132 – Doxylamine succinate and pyridoxine hydrochloride
Doxylamine Succinate 10 mg/1; Pyridoxine Hydrochloride 10 mg/1 · Tablet, Delayed Release · Oral
Product NDC0591-2132
Product details
- Brand name
- Doxylamine succinate and pyridoxine hydrochloride
- Generic name
- Doxylamine succinate and pyridoxine hydrochloride
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Tablet, Delayed Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205811
- Marketed since
- June 21, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Antihistamine; Vitamin B6 Analog
Active ingredients
- Doxylamine Succinate 10 mg/1
- Pyridoxine Hydrochloride 10 mg/1
Uses, dosage, side effects and warnings for Doxylamine succinate and pyridoxine hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0591-2132-01 | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0591-2132-01) | Jun 21, 2019 |
Recalls mentioning this NDC
- D-0461-2022 Feb 9, 2022 · Class II
Failed Dissolution Specification: Dissolution results are below specification limits for the active ingredient
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