Sennosides

UNIISPL

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

Identification

ManufacturerMorepen Laboratories Limited

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
6299300011
30 TABLET in 1 BOTTLE (62993-0001-1)
ndc11
6299300012
100 TABLET in 1 BOTTLE (62993-0001-2)
ndc11
6299300013
250 TABLET in 1 BOTTLE (62993-0001-3)
ndc11
6299300014
1000 TABLET in 1 BOTTLE (62993-0001-4)
ndc11
6299300015
3000 TABLET in 1 BOTTLE (62993-0001-5)
ndc11
6299300016
30000 TABLET in 1 DRUM (62993-0001-6)

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": "62993-0001_461286c9-966a-8847-e063-6394a90a5955",
  "productndc": "62993-0001",
  "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": "20251001",
  "active_numerator_strength": "8.6"
}

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