CKD Bio Corporation
NDC Database

CKD Bio Corporation

NDC Database

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

Bulk Ingredient Drug for Further Processing
  • Total Records 12
  • Latest Marketing Date 2016-10-31
  • Data Source FDA
  • First Marketing Date 1996-11-19
All
12
View
Bulk Ingredient
10
View
Drug for Further Processing
2
View
Company Overview

Company

CKD Bio Corporation

Country

South Korea

Website

Visit Website

Email

dkyim@ckdbio.com

Social Profiles

Company Snapshot

CKD Bio Corporation

CKD building, 8, Chungjeong-ro, Seodaemun-gu, Seoul,

South Korea

www.ckdbio.com/ dkyim@ckdbio.com View on Map
NDC Records ( 12 records )
1998
16 Nov
Bulk Ingredient NDC: 52972-0026

Nonproprietary Name

RIFAMPIN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0026

Substance

RIFAMPIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-11-16

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1996
19 Nov
Bulk Ingredient NDC: 52972-0027

Nonproprietary Name

CYCLOSPORINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0027

Substance

CYCLOSPORINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1996-11-19

End Marketing Date

-

Listing Record Certified Through

2027-12-31

1998
16 Nov
Bulk Ingredient NDC: 52972-0030

Nonproprietary Name

DEMECLOCYCLINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0030

Substance

DEMECLOCYCLINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-11-16

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2003
26 Feb
Bulk Ingredient NDC: 52972-0031

Nonproprietary Name

CLAVULANATE POTASSIUM

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0031

Substance

CLAVULANATE POTASSIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-02-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2005
10 Jun
Drug for Further Processing NDC: 52972-0033

Nonproprietary Name

CLAVULANATE POTASSIUM

Dosage Form

POWDER

Strength

0.5 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

DRUG FOR FURTHER PROCESSING

52972-0033

Substance

CLAVULANATE POTASSIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2005-06-10

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2005
10 Jun
Drug for Further Processing NDC: 52972-0034

Nonproprietary Name

CLAVULANATE POTASSIUM

Dosage Form

POWDER

Strength

0.5 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

DRUG FOR FURTHER PROCESSING

52972-0034

Substance

CLAVULANATE POTASSIUM

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2005-06-10

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2007
12 Sep
Bulk Ingredient NDC: 52972-0035

Nonproprietary Name

ACARBOSE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0035

Substance

ACARBOSE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-09-12

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2010
26 Apr
Bulk Ingredient NDC: 52972-0036

Nonproprietary Name

RIFAMYCIN SODIUM

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0036

Substance

RIFAMYCIN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-04-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2011
07 Jun
Bulk Ingredient NDC: 52972-0037

Nonproprietary Name

MYCOPHENOLATE MOFETIL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0037

Substance

MYCOPHENOLATE MOFETIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-06-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
21 Jun
Bulk Ingredient NDC: 52972-0038

Nonproprietary Name

RIFAMYCIN O

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0038

Substance

RIFAMYCIN O

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-06-21

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2016
31 Oct
Bulk Ingredient NDC: 52972-0039

Nonproprietary Name

Vancomycin Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0039

Substance

VANCOMYCIN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-10-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2016
29 Sep
Bulk Ingredient NDC: 52972-0040

Nonproprietary Name

Tacrolimus

Dosage Form

POWDER

Strength

1 g/g

Labeler

CKD Bio Corporation

Marketing Category

BULK INGREDIENT

52972-0040

Substance

TACROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2016-09-29

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
12 total
  • Bulk Ingredient
  • 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).

Visit FDA NDC Directory
NDC Record Details Preview

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

NDC

52972-0026

Nonproprietary Name

RIFAMPIN

Labeler

CKD Bio Corporation

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

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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