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United States · US · US:52389-155_32c05c2a-5010-0362-e063-6394a90af7cf

Diurex

UNIISPLATC N06BC01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerKobayashi Healthcare International, Inc.
CountryUS (United States)
ATC codeN06BC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    5238915502
    2 BOTTLE, PLASTIC in 1 PACKAGE (52389-155-02) / 80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
  • ndc11
    5238915580
    80 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52389-155-80)
  • ndc11
    5238915590
    1 BOTTLE in 1 CARTON (52389-155-90) / 90 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
3G6A5W338E
CAFFEINE
RxCUI 1886
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "3G6A5W338E",
    "rxcui": "1886",
    "inchikey": "RYYVLZVUVIJVGH-UHFFFAOYSA-N",
    "display_name": "CAFFEINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "874aa629-1330-0c30-e053-2a95a90ac888": {
      "match": "brand_token",
      "title": "DIUREX MAX (PAMABROM) TABLET, FILM COATED [KOBAYASHI HEALTHCARE INTERNATIONAL, INC.]",
      "spl_version": "7",
      "published_date": "2025-05-09"
    }
  },
  "productid": "52389-155_32c05c2a-5010-0362-e063-6394a90af7cf",
  "productndc": "52389-155",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CAFFEINE",
  "proprietary_name": "Diurex",
  "active_ingred_unit": "mg/1",
  "application_number": "M027",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Caffeine",
  "start_marketing_date": "20050901",
  "active_numerator_strength": "100"
}

Related drugs

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