Biogen
NDC Database

Biogen

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Drug for Further Processing
  • Total Records 2
  • Latest Marketing Date 2025-05-18
  • Data Source FDA
  • First Marketing Date 2025-05-18
Company Overview

Company

Biogen

Country

U.S.A

Website

Visit Website

Email

medinfo@biogen.com

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Biogen

225 Binney Street Cambridge, MA 02142

U.S.A

www.biogen.com/ medinfo@biogen.com View on Map
NDC Records ( 2 records )
2025
18 May
Drug for Further Processing NDC: 64406-310

Nonproprietary Name

Nusinersen

Dosage Form

INJECTION, SOLUTION

Strength

5.6 mg/mL

Labeler

Biogen

Marketing Category

DRUG FOR FURTHER PROCESSING

64406-310

Substance

NUSINERSEN

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2025-05-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
18 May
Drug for Further Processing NDC: 64406-311

Nonproprietary Name

Nusinersen

Dosage Form

INJECTION, SOLUTION

Strength

10 mg/mL

Labeler

Biogen

Marketing Category

DRUG FOR FURTHER PROCESSING

64406-311

Substance

NUSINERSEN

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2025-05-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
2 total
  • Drug for Further Processing
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

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NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

64406-310

Nonproprietary Name

Nusinersen

Labeler

Biogen

Dosage Form

INJECTION, SOLUTION

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

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Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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