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United States · US · US:72789-283_2e6f140f-f5e4-32e2-e063-6394a90a54f6
Sennosides
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11727892831010 TABLET in 1 BOTTLE, PLASTIC (72789-283-10)
- ndc11727892833030 TABLET in 1 BOTTLE, PLASTIC (72789-283-30)
Annotations
UNII (FDA Substance ID)
1B5FPI42EN
SENNOSIDES A AND B
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "1B5FPI42EN",
"rxcui": null,
"inchikey": null,
"display_name": "SENNOSIDES A AND B",
"substance_type": "mixture",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"40385b89-a855-4ca2-992a-df5eb677be15": {
"match": "brand_token",
"title": "SENNOSIDES AND DOCUSATE SODIUM TABLET [CARDINAL HEALTH 107, LLC]",
"spl_version": "7",
"published_date": "2026-05-25"
}
},
"productid": "72789-283_2e6f140f-f5e4-32e2-e063-6394a90a54f6",
"productndc": "72789-283",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SENNOSIDES A AND B",
"proprietary_name": "Sennosides",
"active_ingred_unit": "mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Sennosides",
"start_marketing_date": "20200801",
"active_numerator_strength": "8.6"
}Access this data programmatically
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