REBIF REBIDOSE

SPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerEMD Serono, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
4408701881
1 KIT in 1 CARTON (44087-0188-1) * .2 mL in 1 PACKAGE * .5 mL in 1 PACKAGE

Annotations

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "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": "44087-0188_037d2645-544b-41bb-bea8-00b578366ac6",
  "productndc": "44087-0188",
  "dosage_form": "KIT",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": null,
  "proprietary_name": "REBIF REBIDOSE",
  "active_ingred_unit": null,
  "application_number": "BLA103780",
  "marketing_category": "BLA",
  "nonproprietary_name": "INTERFERON BETA-1A",
  "start_marketing_date": "20121221",
  "active_numerator_strength": null
}

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