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United States · US · US:0615-8331_ed210a7f-6612-4caf-851f-c04b02d0cf52

Senexon-S

UNIISPLATC A06AA

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

Identification

ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
CountryUS (United States)
ATC codeA06AA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    0615833105
    15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-05)
  • ndc11
    0615833128
    28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-28)
  • ndc11
    0615833139
    30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8331-39)

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": {
    "c049ef78-cc16-4209-b553-60cead5c9a80": {
      "match": "brand_token",
      "title": "SENEXON-S (DOCUSATE SODIUM 50MG AND SENNOSIDES 8.6MG) TABLET, FILM COATED [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS]",
      "spl_version": "7",
      "published_date": "2025-01-06"
    }
  },
  "productid": "0615-8331_ed210a7f-6612-4caf-851f-c04b02d0cf52",
  "productndc": "0615-8331",
  "dosage_form": "TABLET, FILM COATED",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DOCUSATE SODIUM; SENNOSIDES",
  "proprietary_name": "Senexon-S",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Docusate Sodium 50mg and Sennosides 8.6mg",
  "start_marketing_date": "20191002",
  "active_numerator_strength": "50; 8.6"
}

Related drugs

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