United States · FDA National Drug Code directory
Treda 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
- 83393-749_bf8d9411-58f5-4b37-8af1-6b7142172ef2
- Product NDC
- 83393-749
- Form
- TABLET
- Composition / generic term
- Bismuth subsalicylate
- Labeler
- Laboratorios Sanfer, S.A. de C.V.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20240206
- Source listing expiry
- 20271231
Source-listed ingredients
- BISMUTH SUBSALICYLATE — 525 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (83393-749-08) / 24 TABLET in 1 BOTTLE, PLASTIC · 83393-749-08
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 →