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Diurex Ultra

NDC 52389-155, Caffeine, tablet, film coated, from Kobayashi Healthcare International, Inc..

Product NDC
52389-155
Status
Listed
Labeler
Kobayashi Healthcare International, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
OTC MONOGRAPH DRUG
Application
M027
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/52389-155 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CAFFEINE100 mg/1

Pharmacologic classes

Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]; Methylxanthine [EPC]; Xanthines [CS]

Package NDCNDC-11Package
52389-155-02523890155022 BOTTLE, PLASTIC in 1 PACKAGE (52389-155-02) / 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
52389-155-805238901558080 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52389-155-80)
52389-155-90523890155901 BOTTLE in 1 CARTON (52389-155-90) / 90 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 52389-155 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/52389-155 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 52389-155. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.