NDC 59627-002-07 - AVONEX

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 59627-002
Requested NDC: 59627-002-07
Package NDCs from labels: 59627-002-07, 59627-002-06
Manufacturer: Biogen Inc. | Packaging Coordinators, LLC
Effective date: 2025-11-19
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
AVONEX - Biogen Inc. \| Packaging Coordinators, LLC	Biogen Inc. \| Packaging Coordinators, LLC	2025-11-19	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
59627-002-06	Avonex	1 in 1 CARTON	INJECTION, SOLUTION	1	23
59627-002-07	Avonex	1 in 1 TRAY	INJECTION, SOLUTION	1	23
59627-002-07	Avonex	0.5 mL in 1 SYRINGE	INJECTION, SOLUTION	0.5	23

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59627-002	AVONEX (INTERFERON BETA-1A) KIT AVONEX PEN (INTERFERON BETA-1A) INJECTION, SOLUTION AVONEX (INTERFERON BETA-1A) INJECTION, SOLUTION [BIOGEN INC.]	22	Current NDC, Legacy NDC, 3 package rows	20241115_d70a39cc-de15-4c12-a1ec-8063b69ea0e1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
59627-002-05	EA - Each	59627-002	31696ccb-f2fd-4e79-9d20-4172258cd419	1	2012-07-24
59627-002-06	ML - Milliliter	59627-002	a90c5f27-cfdb-465e-8b90-9c2a34c90f3e	1	2021-09-07
59627-002-07	ML - Milliliter	59627-002	5e7add05-1932-4c66-9876-ff82ad4af6a8	2	2015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
interferon beta-1a	ACTIVE INGREDIENT	XRO4566Q4R	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
ISOPROPYL ALCOHOL	ACTIVE INGREDIENT	ND2M416302	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
interferon beta-1a	ACTIVE MOIETY	XRO4566Q4R	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
ISOPROPYL ALCOHOL	ACTIVE MOIETY	ND2M416302	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
acetic acid	INACTIVE INGREDIENT	Q40Q9N063P	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
Arginine hydrochloride	INACTIVE INGREDIENT	F7LTH1E20Y	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
polysorbate 20	INACTIVE INGREDIENT	7T1F30V5YH	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
Sodium acetate	INACTIVE INGREDIENT	4550K0SC9B	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2
Water	INACTIVE INGREDIENT	059QF0KO0R	AVONEX (INTERFERON BETA-1A) KIT [BIOGEN IDEC INC.]	2

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 49 of 49 · 968 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bio Rock Water	ROCK WATER	BioActive Nutritional, Inc.	178bd16d-0d4f-49d8-866b-8ab3a3c6889d	2018-07-30	Warnings	Exact identifier unii: 059QF0KO0R
Acetic Acid	ACETIC ACID	Baxter Healthcare Corporation	41bc12af-fac5-4ac1-b907-dcb3e35a054c	2018-02-02	Warnings, Adverse reactions	Exact identifier unii: Q40Q9N063P
ENT Essentials All Dry Ear Drying Drops	ISOPROPYL ALCOHOL	Wisconsin Pharmacal Company	5f0bb412-577e-3155-e053-2a91aa0a7f53	2017-11-28	Warnings	Exact identifier unii: ND2M416302
Homeoplex D	GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM,	Supplement Clinic, LLC.	cd6b48ab-3566-484d-8deb-15ef6f8e7e8f	2017-11-01	Warnings	Exact identifier unii: Q40Q9N063P
Glucose Control T015	SYZYGIUM JAMBOLANUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, HYPOPHYSIS SUIS, PANCREAS SUIS, PHASEOLUS, ACETICUM ACIDUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, URANIUM NITRICUM	Guangzhou Renuma Medical Systems Co., Ltd	3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b	2017-10-26	Warnings	Exact identifier unii: Q40Q9N063P
Sterile Water	WATER	Baxter Healthcare Corporation	ef3e79c5-3f58-4b36-a296-64b7d9a651c1	2017-10-17	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Eye Wash	WATER	CVS Pharmacy	049cee29-7ec2-4d5b-8308-f522acde43a7	2017-03-29	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Baxter Healthcare Company	210dc9ab-d6ca-4552-ac19-1be17792d290	2016-05-31	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.