Changzhou Pharmaceutical Factory
NDC Database

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

Changzhou Pharmaceutical Factory

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 6
Latest Marketing Date 2021-01-01
Data Source FDA
First Marketing Date 1981-01-01

Company Overview

Company

Changzhou Pharmaceutical Factory

Country

China

Website

Visit Website

shm@czpharma.com

Social Profiles

Company Snapshot

Changzhou Pharmaceutical Factory

NO. 518 Laodong East Road, Changzhou, Jiangsu, 213018 China

China

www.czpharma.com/ shm@czpharma.com View on Map

NDC Records ( 6 records )

1984

01 Jan

Bulk Ingredient NDC: 55488-0100

Nonproprietary Name

Doxycycline Hyclate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Changzhou Pharmaceutical Factory

Marketing Category

BULK INGREDIENT

55488-0100 View Details

Substance

DOXYCYCLINE HYCLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1984-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

1981

01 Jan

Bulk Ingredient NDC: 55488-0200

Nonproprietary Name

Doxycycline

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Changzhou Pharmaceutical Factory

Marketing Category

BULK INGREDIENT

55488-0200 View Details

Substance

DOXYCYCLINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1981-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

1984

01 Jan

Bulk Ingredient NDC: 55488-0300

Nonproprietary Name

Hydrochlorothiazide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Changzhou Pharmaceutical Factory

Marketing Category

BULK INGREDIENT

55488-0300 View Details

Substance

HYDROCHLOROTHIAZIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1984-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2003

01 Jan

Bulk Ingredient NDC: 55488-0320

Nonproprietary Name

Rosuvastatin Calcium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Changzhou Pharmaceutical Factory

Marketing Category

BULK INGREDIENT

55488-0320 View Details

Substance

ROSUVASTATIN CALCIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2019

01 Jan

Bulk Ingredient NDC: 55488-0600

Nonproprietary Name

Captopril

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Changzhou Pharmaceutical Factory

Marketing Category

BULK INGREDIENT

55488-0600 View Details

Substance

CAPTOPRIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2019-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

2021

01 Jan

Bulk Ingredient NDC: 55488-0700

Nonproprietary Name

Lenalidomide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Changzhou Pharmaceutical Factory

Marketing Category

BULK INGREDIENT

55488-0700 View Details

Substance

LENALIDOMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-01

End Marketing Date

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown

6 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

55488-0100

Nonproprietary Name

Doxycycline Hyclate

Labeler

Changzhou Pharmaceutical Factory

Dosage Form

POWDER

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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