🇺🇸
United States · US · US:63561-0187_3b28e1ec-d284-2f66-e063-6294a90aa7f1
Senna-S
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGranulation Technology, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc116356101871100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-1)
- ndc116356101872220 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-2)
- ndc1163561018731000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63561-0187-3)
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": {
"d148be81-79b4-41f7-b8d8-a0e85b661592": {
"match": "brand_token",
"title": "SENNA-S (DOCUSATE SODIUM AND SENNOSIDES) TABLET [ADVANCED RX LLC]",
"spl_version": "2",
"published_date": "2026-02-19"
}
},
"productid": "63561-0187_3b28e1ec-d284-2f66-e063-6294a90aa7f1",
"productndc": "63561-0187",
"dosage_form": "TABLET, FILM COATED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "Senna-S",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DOCUSATE SODIUM, SENNOSIDES",
"start_marketing_date": "20250729",
"active_numerator_strength": "50; 8.6"
}Related drugs
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