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United States · US · US:52389-306_32732994-0e5d-93a9-e063-6394a90a9c50
Diurex
UNIISPLATC D11AX
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerKobayashi Healthcare International, Inc.
CountryUS (United States)
ATC codeD11AX
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1152389306362 BLISTER PACK in 1 CARTON (52389-306-36) / 18 TABLET, COATED in 1 BLISTER PACK
- ndc1152389306421 BLISTER PACK in 1 CARTON (52389-306-42) / 42 TABLET, COATED in 1 BLISTER PACK (52389-306-01)
- ndc1152389306842 BLISTER PACK in 1 CARTON (52389-306-84) / 42 TABLET, COATED in 1 BLISTER PACK (52389-306-01)
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": "52389-306_32732994-0e5d-93a9-e063-6394a90a9c50",
"productndc": "52389-306",
"dosage_form": "TABLET, COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CAFFEINE; MAGNESIUM SALICYLATE",
"proprietary_name": "Diurex",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M027",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Caffeine, magnesium salicylate",
"start_marketing_date": "20050515",
"active_numerator_strength": "50; 162.5"
}Related drugs
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