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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

  • ndc11
    7278928310
    10 TABLET in 1 BOTTLE, PLASTIC (72789-283-10)
  • ndc11
    7278928330
    30 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"
}

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