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United States · US · US:62993-0002_48f5ab82-91b0-71fa-e063-6294a90a74c9
Docusate Sodium and Sennosides
UNIISPLATC A06AA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMorepen Laboratories Limited
CountryUS (United States)
ATC codeA06AA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 5
- ndc11629930002130 TABLET in 1 BOTTLE (62993-0002-1)
- ndc11629930002260 TABLET in 1 BOTTLE (62993-0002-2)
- ndc116299300023100 TABLET in 1 BOTTLE (62993-0002-3)
- ndc1162993000241000 TABLET in 1 BOTTLE (62993-0002-4)
- ndc1162993000253000 TABLET in 1 BOTTLE (62993-0002-5)
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": "62993-0002_48f5ab82-91b0-71fa-e063-6294a90a74c9",
"productndc": "62993-0002",
"dosage_form": "TABLET",
"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": "20251001",
"active_numerator_strength": "50; 8.6"
}Related drugs
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