Sennosides

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerMarlex Pharmaceuticals Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
1013531401
1 BOTTLE in 1 CARTON (10135-314-01) / 100 TABLET in 1 BOTTLE

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": "10135-314_441efbb5-f993-9e3c-e063-6294a90a8f29",
  "productndc": "10135-314",
  "dosage_form": "TABLET",
  "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": "20181001",
  "active_numerator_strength": "8.6"
}

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