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United States · US · US:80425-0540_3ba0c7e2-c13b-a7d7-e063-6394a90abf07
Prolaxa
UNIISPLATC A06AG10
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAdvanced Rx of Tennessee, LLC
CountryUS (United States)
ATC codeA06AG10
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc118042505401100 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (80425-0540-1)
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": {
"3ba0c0d9-9e6f-a2e6-e063-6394a90a202d": {
"match": "brand_token",
"title": "PROLAXA (DOCUSATE SODIUM 250MG) CAPSULE, LIQUID FILLED [ADVANCED RX OF TENNESSEE, LLC]",
"spl_version": "1",
"published_date": "2025-08-07"
}
},
"productid": "80425-0540_3ba0c7e2-c13b-a7d7-e063-6394a90abf07",
"productndc": "80425-0540",
"dosage_form": "CAPSULE, LIQUID FILLED",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "DOCUSATE SODIUM",
"proprietary_name": "Prolaxa",
"active_ingred_unit": "mg/1",
"application_number": "M007",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Docusate Sodium 250mg",
"start_marketing_date": "20250805",
"active_numerator_strength": "250"
}Related drugs
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