rebif rebidose
Generic: interferon beta-1a
Labeler: emd serono, inc.Drug Facts
Product Profile
Brand Name
rebif rebidose
Generic Name
interferon beta-1a
Labeler
emd serono, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
interferon beta-1a 22 ug/.5mL
Manufacturer
Identifiers & Regulatory
Product NDC
44087-3322
Product ID
44087-3322_037d2645-544b-41bb-bea8-00b578366ac6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA103780
Listing Expiration
2026-12-31
Marketing Start
2012-12-21
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
440873322
Hyphenated Format
44087-3322
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
rebif rebidose (source: ndc)
Generic Name
interferon beta-1a (source: ndc)
Application Number
BLA103780 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 22 ug/.5mL
Packaging
- 12 PACKAGE in 1 CARTON (44087-3322-1) / .5 mL in 1 PACKAGE (44087-3322-9)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["SUBCUTANEOUS"], "spl_id": "037d2645-544b-41bb-bea8-00b578366ac6", "openfda": {"nui": ["M0025715", "N0000191625"], "unii": ["XRO4566Q4R"], "rxcui": ["758025", "758027", "758028", "758029", "758030", "758032", "795748", "795749", "1649994", "1649996", "1650003", "1650004", "1650011", "1650012", "1650268", "1650282"], "spl_set_id": ["c6fcb5d2-8fcd-44fa-a838-b84ee5f44f0f"], "pharm_class_cs": ["Interferon-beta [CS]"], "pharm_class_epc": ["Interferon beta [EPC]"], "manufacturer_name": ["EMD Serono, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 PACKAGE in 1 CARTON (44087-3322-1) / .5 mL in 1 PACKAGE (44087-3322-9)", "package_ndc": "44087-3322-1", "marketing_start_date": "20121221"}], "brand_name": "REBIF REBIDOSE", "product_id": "44087-3322_037d2645-544b-41bb-bea8-00b578366ac6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Interferon beta [EPC]", "Interferon-beta [CS]"], "product_ndc": "44087-3322", "generic_name": "INTERFERON BETA-1A", "labeler_name": "EMD Serono, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "REBIF REBIDOSE", "active_ingredients": [{"name": "INTERFERON BETA-1A", "strength": "22 ug/.5mL"}], "application_number": "BLA103780", "marketing_category": "BLA", "marketing_start_date": "20121221", "listing_expiration_date": "20261231"}