Sekisui Medical Co. Ltd
NDC Database

Sekisui Medical Co. Ltd

NDC Database

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

Bulk Ingredient
  • Total Records 2
  • Latest Marketing Date 2020-06-15
  • Data Source FDA
  • First Marketing Date 1985-03-07
Company Overview

Company

Sekisui Medical Co. Ltd

Country

Japan

Website

Visit Website

Email

http://www.sekisuidiagnostics.com

Social Profiles

LinkedIn
Company Snapshot

Sekisui Medical Co. Ltd

2-1-3, Nihonbashi, Chuo-ku, Tokyo

Japan

www.sekisuimedical.jp/ http://www.sekisuidiagnostics.com View on Map
NDC Records ( 2 records )
2020
15 Jun
Bulk Ingredient NDC: 55152-001

Nonproprietary Name

Clemastine Fumarate

Dosage Form

POWDER

Strength

1 g/g

Labeler

Sekisui Medical Co., Ltd.

Marketing Category

BULK INGREDIENT

55152-001

Substance

CLEMASTINE FUMARATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-06-15

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1985
07 Mar
Bulk Ingredient NDC: 55152-003

Nonproprietary Name

Aminocaproic Acid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Sekisui Medical Co., Ltd.

Marketing Category

BULK INGREDIENT

55152-003

Substance

AMINOCAPROIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1985-03-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
2 total
  • Bulk Ingredient
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

55152-001

Nonproprietary Name

Clemastine Fumarate

Labeler

Sekisui Medical Co., Ltd.

Dosage Form

POWDER

FDA NDC Data

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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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