🇺🇸
United States · US · US:16103-378_0783ba51-f52a-4ac9-a5fe-ae0bfb6ef57c
Senna-S
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPharbest Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc11161033780760 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16103-378-07)
- ndc111610337808100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16103-378-08)
- ndc1116103378111000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16103-378-11)
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": "16103-378_0783ba51-f52a-4ac9-a5fe-ae0bfb6ef57c",
"productndc": "16103-378",
"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": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Sennosides 8.6mg and Docusate Sodium 50mg",
"start_marketing_date": "20181105",
"active_numerator_strength": "50; 8.6"
}Related drugs
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