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United States · US · US:72606-049_bacf86b8-9d2f-45d2-9c35-4f619ea494aa
Tocilizumab-anoh
UNIISPLATC L04AC07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCELLTRION USA, Inc.
CountryUS (United States)
ATC codeL04AC07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1172606049011 VIAL, SINGLE-DOSE in 1 CARTON (72606-049-01) / 10 mL in 1 VIAL, SINGLE-DOSE
- ndc1172606049024 VIAL, SINGLE-DOSE in 1 CARTON (72606-049-02) / 10 mL in 1 VIAL, SINGLE-DOSE
Annotations
UNII (FDA Substance ID)
I031V2H011
TOCILIZUMAB
RxCUI 612865
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "I031V2H011",
"rxcui": "612865",
"inchikey": null,
"display_name": "TOCILIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"60381a7e-d7ae-4384-925d-c19c418d1663": {
"match": "brand_token",
"title": "TOCILIZUMAB-ANOH (TOCILIZUMAB) INJECTION, SOLUTION, CONCENTRATE [CELLTRION USA, INC.]",
"spl_version": "4",
"published_date": "2026-01-23"
}
},
"productid": "72606-049_bacf86b8-9d2f-45d2-9c35-4f619ea494aa",
"productndc": "72606-049",
"dosage_form": "INJECTION, SOLUTION, CONCENTRATE",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "TOCILIZUMAB",
"proprietary_name": "Tocilizumab-anoh",
"active_ingred_unit": "mg/10mL",
"application_number": "BLA761420",
"marketing_category": "BLA",
"nonproprietary_name": "tocilizumab",
"start_marketing_date": "20250126",
"active_numerator_strength": "200"
}Related drugs
Other records sharing ATC code L04AC07.
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