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United States · US · US:52389-249_3287c676-c9cc-273e-e063-6294a90a9c9b
Diurex
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKobayashi Healthcare International, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 6
- ndc1152389249104 BLISTER PACK in 1 CARTON (52389-249-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1152389249241 BLISTER PACK in 1 CARTON (52389-249-24) / 24 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1152389249303 BLISTER PACK in 1 CARTON (52389-249-30) / 10 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1152389249482 BLISTER PACK in 1 CARTON (52389-249-48) / 24 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1152389249505 BLISTER PACK in 1 CARTON (52389-249-50) / 10 TABLET, FILM COATED in 1 BLISTER PACK
- ndc1152389249723 BLISTER PACK in 1 CARTON (52389-249-72) / 24 TABLET, FILM COATED in 1 BLISTER PACK
Annotations
UNII (FDA Substance ID)
UA8U0KJM72
PAMABROM
RxCUI 54365
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "UA8U0KJM72",
"rxcui": "54365",
"inchikey": "ATOTUUBRFJHZQG-UHFFFAOYSA-N",
"display_name": "PAMABROM",
"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": "52389-249_3287c676-c9cc-273e-e063-6294a90a9c9b",
"productndc": "52389-249",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "PAMABROM",
"proprietary_name": "Diurex",
"active_ingred_unit": "mg/1",
"application_number": "M027",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Pamabrom",
"start_marketing_date": "19951220",
"active_numerator_strength": "50"
}Access this data programmatically
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