Nipro Pharma Corporation
NDC Database

Nipro Pharma Corporation

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 2025-04-01
  • Data Source FDA
  • First Marketing Date 2018-11-23
Company Overview

Company

Nipro Pharma Corporation

Country

Japan

Website

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Company Snapshot

Nipro Pharma Corporation

2-2-7, Dosho-machi, Chuo-ku, Osaka, 541-0045, Japan

Japan

www.np.nipro-pharma.co.jp/english/index.php View on Map
NDC Records ( 2 records )
2018
23 Nov
Drug for Further Processing NDC: 72122-001

Nonproprietary Name

gefitinib tablets

Dosage Form

TABLET

Strength

250 mg/1

Labeler

Nipro Pharma Corporation

Marketing Category

DRUG FOR FURTHER PROCESSING

72122-001

Substance

GEFITINIB

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2018-11-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
01 Apr
Drug for Further Processing NDC: 72122-004

Nonproprietary Name

Ceftobiprole Medocaril Sodium for Injection

Dosage Form

INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Strength

500 mg/mL

Labeler

Nipro Pharma Corporation

Marketing Category

DRUG FOR FURTHER PROCESSING

72122-004

Substance

CEFTOBIPROLE MEDOCARIL SODIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2025-04-01

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

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NDC

72122-001

Nonproprietary Name

gefitinib tablets

Labeler

Nipro Pharma Corporation

Dosage Form

TABLET

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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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