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United States · US · US:35916-0477_50038665-465f-1bc7-e063-6394a90abd16
Docusate Sodium and Sennosides
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSOFTGEL HEALTHCARE PRIVATE LIMITED
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1135916047712 BAG in 1 BOX (35916-0477-1) / 1500 CAPSULE, LIQUID FILLED in 1 BAG
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": "35916-0477_50038665-465f-1bc7-e063-6394a90abd16",
"productndc": "35916-0477",
"dosage_form": "CAPSULE, LIQUID FILLED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM; SENNOSIDES",
"proprietary_name": "Docusate Sodium and Sennosides",
"active_ingred_unit": "mg/1; mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Docusate Sodium and Sennosides",
"start_marketing_date": "20260116",
"active_numerator_strength": "50; 8.6"
}Related drugs
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