United States · FDA National Drug Code directory
Diurex 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
- 52389-155_32c05c2a-5010-0362-e063-6394a90af7cf
- Product NDC
- 52389-155
- Form
- TABLET, FILM COATED
- Composition / generic term
- Caffeine
- Labeler
- Kobayashi Healthcare International, Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20050901
- Source listing expiry
- 20261231
Source-listed ingredients
- CAFFEINE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BOTTLE, PLASTIC in 1 PACKAGE (52389-155-02) / 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC · 52389-155-02
- 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52389-155-80) · 52389-155-80
- 1 BOTTLE in 1 CARTON (52389-155-90) / 90 TABLET, FILM COATED in 1 BOTTLE · 52389-155-90
Source and coverage
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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.
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