kineret

Generic: anakinra

Labeler: swedish orphan biovitrum ab (publ)
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name kineret
Generic Name anakinra
Labeler swedish orphan biovitrum ab (publ)
Dosage Form INJECTION, SOLUTION
Routes
SUBCUTANEOUS
Active Ingredients

anakinra 100 mg/.67mL

Manufacturer
Swedish Orphan Biovitrum AB (publ)

Identifiers & Regulatory

Product NDC 66658-234
Product ID 66658-234_5f01b0c0-d7b9-44a8-8405-983bbda95ef1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA103950
Listing Expiration 2026-12-31
Marketing Start 2009-12-15

Pharmacologic Class

Established (EPC)
interleukin-1 receptor antagonist [epc]
Mechanism of Action
interleukin 1 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 66658234
Hyphenated Format 66658-234

Supplemental Identifiers

RxCUI
727711 727714
UNII
9013DUQ28K
NUI
N0000175709 N0000175710

Packaging Origin

Original Packager
true

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 kineret (source: ndc)
Generic Name anakinra (source: ndc)
Application Number BLA103950 (source: ndc)
Routes
SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 100 mg/.67mL
source: ndc
Packaging
  • 7 SYRINGE, GLASS in 1 CARTON (66658-234-07) / .67 mL in 1 SYRINGE, GLASS
  • 4 CARTON in 1 CASE (66658-234-28) / 7 SYRINGE, GLASS in 1 CARTON / .67 mL in 1 SYRINGE, GLASS
source: ndc

Packages (2)

66658-234-07 7 SYRINGE, GLASS in 1 CARTON (66658-234-07) / .67 mL in 1 SYRINGE, GLASS 66658-234-28 4 CARTON in 1 CASE (66658-234-28) / 7 SYRINGE, GLASS in 1 CARTON / .67 mL in 1 SYRINGE, GLASS

Ingredients (1)

anakinra (100 mg/.67mL)

Linked Drug Pages (1)

Kineret ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "5f01b0c0-d7b9-44a8-8405-983bbda95ef1", "openfda": {"nui": ["N0000175709", "N0000175710"], "unii": ["9013DUQ28K"], "rxcui": ["727711", "727714"], "spl_set_id": ["d9d74915-6606-4570-9c52-c4001d3177de"], "pharm_class_epc": ["Interleukin-1 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Interleukin 1 Receptor Antagonists [MoA]"], "manufacturer_name": ["Swedish Orphan Biovitrum AB (publ)"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "7 SYRINGE, GLASS in 1 CARTON (66658-234-07)  / .67 mL in 1 SYRINGE, GLASS", "package_ndc": "66658-234-07", "marketing_start_date": "20091215"}, {"sample": false, "description": "4 CARTON in 1 CASE (66658-234-28)  / 7 SYRINGE, GLASS in 1 CARTON / .67 mL in 1 SYRINGE, GLASS", "package_ndc": "66658-234-28", "marketing_start_date": "20091215"}], "brand_name": "Kineret", "product_id": "66658-234_5f01b0c0-d7b9-44a8-8405-983bbda95ef1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Interleukin 1 Receptor Antagonists [MoA]", "Interleukin-1 Receptor Antagonist [EPC]"], "product_ndc": "66658-234", "generic_name": "anakinra", "labeler_name": "Swedish Orphan Biovitrum AB (publ)", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Kineret", "active_ingredients": [{"name": "ANAKINRA", "strength": "100 mg/.67mL"}], "application_number": "BLA103950", "marketing_category": "BLA", "marketing_start_date": "20091215", "listing_expiration_date": "20261231"}