Siegfried AG Drug For Further Processing
NDC Database

Siegfried AG Drug For Further Processing

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 2023-06-16
  • Data Source FDA
  • First Marketing Date 2023-04-01
All
54
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Bulk Ingredient
52
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Drug for Further Processing
2
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Company Overview

Company

Siegfried AG Drug For Further Processing

Country

Switzerland

Website

Visit Website

Email

info@siegfried.ch

Social Profiles

LinkedIn X / Twitter
Company Snapshot

Siegfried AG Drug For Further Processing

Untere Bruehlstrasse 4, 4800 Zofingen

Switzerland

www.siegfried.ch/ info@siegfried.ch View on Map
NDC Records ( 2 records )
2023
01 Apr
Drug for Further Processing NDC: 17205-205

Nonproprietary Name

THALIDOMIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

DRUG FOR FURTHER PROCESSING

17205-205

Substance

THALIDOMIDE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2023-04-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
16 Jun
Drug for Further Processing NDC: 17205-628

Nonproprietary Name

ZANUBRUTINIB

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Siegfried AG

Marketing Category

DRUG FOR FURTHER PROCESSING

17205-628

Substance

ZANUBRUTINIB

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2023-06-16

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

17205-205

Nonproprietary Name

THALIDOMIDE

Labeler

Siegfried AG

Dosage Form

POWDER

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

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