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United States · US · US:49873-404_0b54b2d1-83e7-3a18-e063-6394a90a5b58
Sankaijo
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSato Pharmaceutical Co., Ltd.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1149873404011 BOTTLE in 1 CARTON (49873-404-01) / 150 TABLET in 1 BOTTLE
Annotations
UNII (FDA Substance ID)
F05Q2T2JA0
DOCUSATE SODIUM
RxCUI 71722
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "F05Q2T2JA0",
"rxcui": "71722",
"inchikey": "APSBXTVYXVQYAB-UHFFFAOYSA-M",
"display_name": "DOCUSATE SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"83c0d52b-f7e2-40b0-a01b-1ccee78f8f1b": {
"match": "brand_token",
"title": "SANKAIJO (DOCUSATE SODIUM, SENNOSIDES) TABLET [SATO PHARMACEUTICAL CO., LTD.]",
"spl_version": "11",
"published_date": "2023-11-30"
}
},
"productid": "49873-404_0b54b2d1-83e7-3a18-e063-6394a90a5b58",
"productndc": "49873-404",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "Sankaijo",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "docusate sodium, sennosides",
"start_marketing_date": "20021220",
"active_numerator_strength": "8.33; 1.36"
}Related drugs
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