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United States · US · US:0006-3026_2251fde0-831a-4f47-a325-0859f3a235e7
KEYTRUDA
UNIISPLATC L01FF02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMerck Sharp & Dohme LLC
CountryUS (United States)
ATC codeL01FF02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1100063026021 VIAL in 1 CARTON (0006-3026-02) / 4 mL in 1 VIAL (0006-3026-01)
- ndc1100063026042 VIAL in 1 CARTON (0006-3026-04) / 4 mL in 1 VIAL (0006-3026-01)
Annotations
UNII (FDA Substance ID)
DPT0O3T46P
PEMBROLIZUMAB
RxCUI 1547545
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "DPT0O3T46P",
"rxcui": "1547545",
"inchikey": null,
"display_name": "PEMBROLIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"9333c79b-d487-4538-a9f0-71b91a02b287": {
"match": "brand_token",
"title": "KEYTRUDA (PEMBROLIZUMAB) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION KEYTRUDA (PEMBROLIZUMAB) INJECTION, SOLUTION [MERCK SHARP & DOHME LLC ]",
"spl_version": "225",
"published_date": "2026-05-21"
}
},
"productid": "0006-3026_2251fde0-831a-4f47-a325-0859f3a235e7",
"productndc": "0006-3026",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "PEMBROLIZUMAB",
"proprietary_name": "KEYTRUDA",
"active_ingred_unit": "mg/mL",
"application_number": "BLA125514",
"marketing_category": "BLA",
"nonproprietary_name": "pembrolizumab",
"start_marketing_date": "20150115",
"active_numerator_strength": "25"
}Related drugs
Other records sharing ATC code L01FF02.
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