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United States · US · US:76420-918_2d9d8f71-cc36-459a-e063-6394a90acf8e

Sennosides and Docusate Sodium

UNIISPLATC A06AA

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

Identification

ManufacturerAsclemed USA, Inc.
CountryUS (United States)
ATC codeA06AA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    7642091801
    100 TABLET in 1 BOTTLE (76420-918-01)
  • ndc11
    7642091830
    30 TABLET in 1 BOTTLE (76420-918-30)
  • ndc11
    7642091860
    60 TABLET in 1 BOTTLE (76420-918-60)
  • ndc11
    7642091890
    90 TABLET in 1 BOTTLE (76420-918-90)

Annotations

UNII (FDA Substance ID)
F05Q2T2JA0
DOCUSATE SODIUM
RxCUI 71722
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "F05Q2T2JA0",
    "rxcui": "71722",
    "inchikey": "APSBXTVYXVQYAB-UHFFFAOYSA-M",
    "display_name": "DOCUSATE SODIUM",
    "substance_type": "chemical",
    "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": "76420-918_2d9d8f71-cc36-459a-e063-6394a90acf8e",
  "productndc": "76420-918",
  "dosage_form": "TABLET",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DOCUSATE SODIUM; SENNOSIDES",
  "proprietary_name": "Sennosides and Docusate Sodium",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "M007",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Sennosides, Docusate Sodium",
  "start_marketing_date": "20200801",
  "active_numerator_strength": "50; 8.6"
}

Related drugs

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