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United States · US · US:44087-3344_037d2645-544b-41bb-bea8-00b578366ac6
REBIF REBIDOSE
UNIISPLATC L03AB07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerEMD Serono, Inc.
CountryUS (United States)
ATC codeL03AB07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11440873344112 PACKAGE in 1 CARTON (44087-3344-1) / .5 mL in 1 PACKAGE (44087-3344-9)
Annotations
UNII (FDA Substance ID)
XRO4566Q4R
INTERFERON BETA-1A
RxCUI 75917
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "XRO4566Q4R",
"rxcui": "75917",
"inchikey": null,
"display_name": "INTERFERON BETA-1A",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBCUTANEOUS",
"spl_meta": {
"c6fcb5d2-8fcd-44fa-a838-b84ee5f44f0f": {
"match": "brand_token",
"title": "REBIF (INTERFERON BETA-1A) KIT REBIF REBIDOSE (INTERFERON BETA-1A) KIT REBIF (INTERFERON BETA-1A ) INJECTION, SOLUTION REBIF (INTERFERON BETA-1A) INJECTION, SOLUTION REBIF REBIDOSE (INTERFERON BETA-1A ) INJECTION, SOLUTION [EMD SERONO, INC.]",
"spl_version": "27",
"published_date": "2025-09-29"
}
},
"productid": "44087-3344_037d2645-544b-41bb-bea8-00b578366ac6",
"productndc": "44087-3344",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "INTERFERON BETA-1A",
"proprietary_name": "REBIF REBIDOSE",
"active_ingred_unit": "ug/.5mL",
"application_number": "BLA103780",
"marketing_category": "BLA",
"nonproprietary_name": "INTERFERON BETA-1A",
"start_marketing_date": "20121221",
"active_numerator_strength": "44"
}Related drugs
Other records sharing ATC code L03AB07.
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