United States · FDA National Drug Code directory
sleep aid ultra
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 79481-0096_d802f1ad-a820-42ba-8bd6-b35499deb7a2
- Product NDC
- 79481-0096
- Form
- TABLET
- Composition / generic term
- Doxylamine Succinate
- Labeler
- Meijer, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220729
- Source listing expiry
- 20261231
Source-listed ingredients
- DOXYLAMINE SUCCINATE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 24 BLISTER PACK in 1 CARTON (79481-0096-0) / 1 TABLET in 1 BLISTER PACK · 79481-0096-0
- 12 BLISTER PACK in 1 CARTON (79481-0096-1) / 1 TABLET in 1 BLISTER PACK · 79481-0096-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →