Tianjin Tianyao Pharmaceuticals Co., Ltd.
NDC Database

Tianjin Tianyao Pharmaceuticals Co., Ltd.

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 11
  • Latest Marketing Date 2022-01-20
  • Data Source FDA
  • First Marketing Date 2012-02-01
All
11
View
Bulk Ingredient
8
View
Drug for Further Processing
3
View
Company Overview

Company

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Country

China

Website

Visit Website

Email

lixm1@tjpc.com.cn

Social Profiles

Company Snapshot

Tianjin Tianyao Pharmaceuticals Co., Ltd.

No.19, XINYE 9th Street, West Area of Tianjin Economic-Technological Development Area (TEDA), Tianjin  300 462

China

www.tjpc.com.cn/ lixm1@tjpc.com.cn View on Map
NDC Records ( 11 records )
2012
01 Feb
Bulk Ingredient NDC: 57582-003

Nonproprietary Name

Prednisone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

DRUG FOR FURTHER PROCESSING

57582-003

Substance

PREDNISONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-02-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2017
01 Feb
Bulk Ingredient NDC: 57582-004

Nonproprietary Name

Prednisolone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

DRUG FOR FURTHER PROCESSING

57582-004

Substance

PREDNISOLONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-02-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
01 Jul
Bulk Ingredient NDC: 57582-011

Nonproprietary Name

Methylprednisolone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

DRUG FOR FURTHER PROCESSING

57582-011

Substance

METHYLPREDNISOLONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-07-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
10 Jun
Bulk Ingredient NDC: 57582-012

Nonproprietary Name

Methylprednisolone hemisuccinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

BULK INGREDIENT

57582-012

Substance

METHYLPREDNISOLONE HEMISUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-06-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
20 Jan
Bulk Ingredient NDC: 57582-013

Nonproprietary Name

Hydrocortisone

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

BULK INGREDIENT

57582-013

Substance

HYDROCORTISONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-01-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
20 Jan
Bulk Ingredient NDC: 57582-015

Nonproprietary Name

Dexamethasone Sodium Phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

BULK INGREDIENT

57582-015

Substance

DEXAMETHASONE SODIUM PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
01 Jan
Bulk Ingredient NDC: 57582-018

Nonproprietary Name

Triamcinolone Acetonide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

BULK INGREDIENT

57582-018

Substance

TRIAMCINOLONE ACETONIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
20 May
Bulk Ingredient NDC: 57582-030

Nonproprietary Name

Spironolactone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

DRUG FOR FURTHER PROCESSING

57582-030

Substance

SPIRONOLACTONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-05-20

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Dec
Drug for Further Processing NDC: 57582-032

Nonproprietary Name

Celecoxib

Dosage Form

POWDER

Strength

25 kg/25kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

DRUG FOR FURTHER PROCESSING

57582-032

Substance

CELECOXIB

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2020-12-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
10 Jun
Drug for Further Processing NDC: 57582-040

Nonproprietary Name

Deflazacort

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

DRUG FOR FURTHER PROCESSING

57582-040

Substance

DEFLAZACORT

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2021-06-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
01 Oct
Drug for Further Processing NDC: 57582-041

Nonproprietary Name

Trilostane

Dosage Form

POWDER

Strength

5 kg/5kg

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Marketing Category

DRUG FOR FURTHER PROCESSING

57582-041

Substance

TRILOSTANE

Product Type

DRUG FOR FURTHER PROCESSING

DEA Schedule

Start Marketing Date

2021-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
11 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).

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NDC Record Details Preview

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

NDC

57582-003

Nonproprietary Name

Prednisone

Labeler

Tianjin Tianyao Pharmaceuticals Co., Ltd.

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

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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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