CMIC CMO CO., LTD
NDC Database

CMIC CMO CO., LTD

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 2018-05-24
  • Data Source FDA
  • First Marketing Date 2018-05-24
Company Overview

Company

CMIC CMO CO., LTD

Country

Japan

Social Profiles

Company Snapshot

CMIC CMO CO., LTD

K1-1-1, Shibaura, Minato-ku, Tokyo 105-0023

Japan

www.cmic-cmo.com/e/ cmo-bd@cmic.co.jp View on Map
NDC Records ( 2 records )
2018
24 May
Drug for Further Processing NDC: 51434-1230

Nonproprietary Name

Tacrolimus

Dosage Form

GRANULE, FOR SUSPENSION

Strength

0.2 mg/1

Labeler

CMIC CMO CO., LTD.

Marketing Category

DRUG FOR FURTHER PROCESSING

51434-1230

Substance

TACROLIMUS

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2018-05-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
24 May
Drug for Further Processing NDC: 51434-1330

Nonproprietary Name

Tacrolimus

Dosage Form

GRANULE, FOR SUSPENSION

Strength

1 mg/1

Labeler

CMIC CMO CO., LTD.

Marketing Category

DRUG FOR FURTHER PROCESSING

51434-1330

Substance

TACROLIMUS

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2018-05-24

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

51434-1230

Nonproprietary Name

Tacrolimus

Labeler

CMIC CMO CO., LTD.

Dosage Form

GRANULE, FOR SUSPENSION

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

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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