Sennosides

UNIISPL

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

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 7

ndc11
7133526601
100 TABLET, FILM COATED in 1 BOTTLE (71335-2660-1)
ndc11
7133526602
60 TABLET, FILM COATED in 1 BOTTLE (71335-2660-2)
ndc11
7133526603
120 TABLET, FILM COATED in 1 BOTTLE (71335-2660-3)
ndc11
7133526604
56 TABLET, FILM COATED in 1 BOTTLE (71335-2660-4)
ndc11
7133526605
30 TABLET, FILM COATED in 1 BOTTLE (71335-2660-5)
ndc11
7133526606
90 TABLET, FILM COATED in 1 BOTTLE (71335-2660-6)
ndc11
7133526607
10 TABLET, FILM COATED in 1 BOTTLE (71335-2660-7)

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": "71335-2660_644bf13d-7b0c-4042-b8a2-d017af5ab911",
  "productndc": "71335-2660",
  "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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