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United States · US · US:72789-399_4bc0d603-ca55-d405-e063-6394a90a1ac7
DOCUSATE SODIUM
UNIISPLATC A06AG10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerPD-Rx Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeA06AG10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11727893993030 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (72789-399-30)
- ndc11727893996060 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (72789-399-60)
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": "72789-399_4bc0d603-ca55-d405-e063-6394a90a1ac7",
"productndc": "72789-399",
"dosage_form": "CAPSULE, LIQUID FILLED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM",
"proprietary_name": "DOCUSATE SODIUM",
"active_ingred_unit": "mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DOCUSATE SODIUM",
"start_marketing_date": "20221115",
"active_numerator_strength": "100"
}Related drugs
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