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United States · US · US:55513-132_94338615-f26e-4373-93ce-106894c98a87
Kanjinti
UNIISPLATC L01FD01
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmgen, Inc
CountryUS (United States)
ATC codeL01FD01
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1155513132011 VIAL, MULTI-DOSE in 1 CARTON (55513-132-01) / 20 mL in 1 VIAL, MULTI-DOSE
- ndc1155513132211 VIAL, MULTI-DOSE in 1 CARTON (55513-132-21) / 20 mL in 1 VIAL, MULTI-DOSE
Annotations
UNII (FDA Substance ID)
P188ANX8CK
TRASTUZUMAB
RxCUI 224905
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "P188ANX8CK",
"rxcui": "224905",
"inchikey": null,
"display_name": "TRASTUZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"9a94f5b2-b84e-4987-8ea1-c4346db5a5fa": {
"match": "brand_token",
"title": "KANJINTI (TRASTUZUMAB-ANNS) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [AMGEN, INC]",
"spl_version": "22",
"published_date": "2026-03-17"
}
},
"productid": "55513-132_94338615-f26e-4373-93ce-106894c98a87",
"productndc": "55513-132",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "TRASTUZUMAB",
"proprietary_name": "Kanjinti",
"active_ingred_unit": "mg/20mL",
"application_number": "BLA761073",
"marketing_category": "BLA",
"nonproprietary_name": "trastuzumab-anns",
"start_marketing_date": "20190611",
"active_numerator_strength": "420"
}Related drugs
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