Docusate Sodium Oral Liquid

UNIISPLATC A06AG10

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

Identification

ManufacturerKesin Pharma Corporation

CountryUS (United States)

ATC codeA06AG10

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8103302250
100 CUP, UNIT-DOSE in 1 CASE (81033-022-50) / 10 mL in 1 CUP, UNIT-DOSE (81033-022-10)

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": {
    "492b6d37-47cf-3a28-e063-6294a90a2a18": {
      "match": "brand_token",
      "title": "DOCUSATE SODIUM LIQUID (DOCUSATE SODIUM.50MG/5ML) SOLUTION [ALDAMA PHARMACEUTICALS, INC]",
      "spl_version": "2",
      "published_date": "2026-06-02"
    }
  },
  "productid": "81033-022_331277b8-8305-d082-e063-6394a90a4dd3",
  "productndc": "81033-022",
  "dosage_form": "LIQUID",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "DOCUSATE SODIUM",
  "proprietary_name": "Docusate Sodium Oral Liquid",
  "active_ingred_unit": "mg/10mL",
  "application_number": "M007",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Docusate Sodium Oral Liquid",
  "start_marketing_date": "20250401",
  "active_numerator_strength": "100"
}

Related drugs

Other records sharing ATC code A06AG10.

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