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United States · US · US:42806-018_fb793a0a-affa-4f9a-a5b4-aa1c84aa475e
SULINDAC
UNIISPLATC M01AB02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEpic Pharma, LLC
CountryUS (United States)
ATC codeM01AB02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc114280601801100 TABLET in 1 BOTTLE (42806-018-01)
- ndc114280601805500 TABLET in 1 BOTTLE (42806-018-05)
- ndc1142806018101000 TABLET in 1 BOTTLE (42806-018-10)
Annotations
UNII (FDA Substance ID)
184SNS8VUH
SULINDAC
RxCUI 10237
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "184SNS8VUH",
"rxcui": "10237",
"inchikey": "MLKXDPUZXIRXEP-MFOYZWKCSA-N",
"display_name": "SULINDAC",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"6041acc2-5e8a-4d3c-bf50-7e9447748e2b": {
"match": "brand_token",
"title": "SULINDAC TABLET [A-S MEDICATION SOLUTIONS]",
"spl_version": "16",
"published_date": "2026-05-11"
}
},
"productid": "42806-018_fb793a0a-affa-4f9a-a5b4-aa1c84aa475e",
"productndc": "42806-018",
"dosage_form": "TABLET",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "SULINDAC",
"proprietary_name": "SULINDAC",
"active_ingred_unit": "mg/1",
"application_number": "ANDA072710",
"marketing_category": "ANDA",
"nonproprietary_name": "SULINDAC",
"start_marketing_date": "20100125",
"active_numerator_strength": "150"
}Related drugs
Other records sharing ATC code M01AB02.
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