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United States Β· US Β· US:0904-7252_289eb036-6a1f-4d89-e063-6394a90ac159

Sennosides

UNIISPL

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerMajor Pharmaceuticals
CountryUS (United States)
ATC codeβ€”
Dispensingβ€”
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs Β· 3

  • ndc11
    0904725260
    100 TABLET, FILM COATED in 1 BOTTLE (0904-7252-60)
  • ndc11
    0904725261
    10 BLISTER PACK in 1 BOX, UNIT-DOSE (0904-7252-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    0904725280
    1000 TABLET, FILM COATED in 1 BOTTLE (0904-7252-80)

Annotations

UNII (FDA Substance ID)
3FYP5M0IJX
SENNOSIDES
RxCUI 36387
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "3FYP5M0IJX",
    "rxcui": "36387",
    "inchikey": null,
    "display_name": "SENNOSIDES",
    "substance_type": "structurallyDiverse",
    "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": "0904-7252_289eb036-6a1f-4d89-e063-6394a90ac159",
  "productndc": "0904-7252",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "SENNOSIDES",
  "proprietary_name": "Sennosides",
  "active_ingred_unit": "mg/1",
  "application_number": "M007",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Sennosides",
  "start_marketing_date": "20220517",
  "active_numerator_strength": "8.6"
}

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Sennosides (US) β€” Drug Database