Chirogate International
NDC Database

Name: Chirogate International NDC Database
Creator: U.S. Food and Drug Administration
License: https://www.fda.gov/
Keywords: Chirogate International, NDC, National Drug Code, FDA NDC, pharmaceutical products

Chirogate International

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 13
Latest Marketing Date 2014-01-01
Data Source FDA
First Marketing Date 2003-01-01

Company Overview

Company

Chirogate International

Country

Taiwan

Website

Visit Website

sales@chirogate.com

Social Profiles

Company Snapshot

Chirogate International

No.2, Shih 4th Rd., Youth Industrial Park, Yangmei Dist., Taoyuan City

Taiwan

www.chirogate.com/about.html sales@chirogate.com View on Map

NDC Records ( 13 records )

2005

01 Jan

Bulk Ingredient NDC: 68245-0001

Nonproprietary Name

Misoprostol

Dosage Form

LIQUID

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0001 View Details

Substance

MISOPROSTOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2003

01 Jan

Bulk Ingredient NDC: 68245-0002

Nonproprietary Name

Latanoprost

Dosage Form

LIQUID

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0002 View Details

Substance

LATANOPROST

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2007

01 Jan

Bulk Ingredient NDC: 68245-0003

Nonproprietary Name

Travoprost

Dosage Form

LIQUID

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0003 View Details

Substance

TRAVOPROST

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2007

01 Jan

Bulk Ingredient NDC: 68245-0004

Nonproprietary Name

Bimatoprost

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0004 View Details

Substance

BIMATOPROST

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2005

01 Jan

Bulk Ingredient NDC: 68245-0005

Nonproprietary Name

Epoprostenol Sodium

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0005 View Details

Substance

EPOPROSTENOL SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2005

01 Jan

Bulk Ingredient NDC: 68245-0006

Nonproprietary Name

Misoprostol 1% HPMC Dispersion

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0006 View Details

Substance

MISOPROSTOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2005

01 Jan

Bulk Ingredient NDC: 68245-0007

Nonproprietary Name

Alprostadil

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0007 View Details

Substance

ALPROSTADIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2010

01 Jan

Bulk Ingredient NDC: 68245-0008

Nonproprietary Name

Treprostinil

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0008 View Details

Substance

TREPROSTINIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2010

01 Jan

Bulk Ingredient NDC: 68245-0009

Nonproprietary Name

Treprostinil Sodium

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0009 View Details

Substance

TREPROSTINIL SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2010

01 Jan

Bulk Ingredient NDC: 68245-0010

Nonproprietary Name

Treprostinil Diolamine

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0010 View Details

Substance

TREPROSTINIL DIOLAMINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2010

01 Jan

Bulk Ingredient NDC: 68245-0011

Nonproprietary Name

Lubiprostone

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0011 View Details

Substance

LUBIPROSTONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2010

01 Jan

Bulk Ingredient NDC: 68245-0012

Nonproprietary Name

Tafluprost

Dosage Form

LIQUID

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0012 View Details

Substance

TAFLUPROST

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2014

01 Jan

Bulk Ingredient NDC: 68245-0014

Nonproprietary Name

Hexadecyl Treprostinil

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chirogate International Inc

Marketing Category

BULK INGREDIENT

68245-0014 View Details

Substance

TREPROSTINIL HEXADECYL ESTER

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown

13 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).

Visit FDA NDC Directory

NDC Record Details Preview

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

NDC

68245-0001

Nonproprietary Name

Misoprostol

Labeler

Chirogate International Inc

Dosage Form

LIQUID

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

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