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United States · US · US:80136-555_45263661-3ac1-6283-e063-6394a90ac1ec
SENNA-PLUS
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerHeartland Pharma Co.
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118013655501100 TABLET in 1 BOTTLE (80136-555-01)
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": {
"d7146449-c43e-460a-9ae0-aa1966eaa3b6": {
"match": "brand_token",
"title": "SENNA-PLUS (SENNOSIDES AND DOCUSATE SODIUM) TABLET [PREFERRED PHARMACEUTICALS INC.]",
"spl_version": "2",
"published_date": "2026-01-23"
}
},
"productid": "80136-555_45263661-3ac1-6283-e063-6394a90ac1ec",
"productndc": "80136-555",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "SENNA-PLUS",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "505G(a)(3)",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Sennosides and Docusate Sodium",
"start_marketing_date": "20221201",
"active_numerator_strength": "50; 8.6"
}Related drugs
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