United States · FDA National Drug Code directory
Sominex
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
- 63029-554_322a3f7f-6a0f-43b9-9819-9ec52e856404
- Product NDC
- 63029-554
- Form
- TABLET, FILM COATED
- Composition / generic term
- DIPHENHYDRAMINE HYDROCHLORIDE
- Labeler
- Medtech Products Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20120601
- Source listing expiry
- 20261231
Source-listed ingredients
- DIPHENHYDRAMINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 9 BLISTER PACK in 1 BOX (63029-554-01) / 8 TABLET, FILM COATED in 1 BLISTER PACK · 63029-554-01
- 2 BLISTER PACK in 1 BOX (63029-554-16) / 8 TABLET, FILM COATED in 1 BLISTER PACK · 63029-554-16
- 4 BLISTER PACK in 1 BOX (63029-554-32) / 8 TABLET, FILM COATED in 1 BLISTER PACK · 63029-554-32
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 →