Henan Lihua Pharmaceutical
NDC Database

Henan Lihua Pharmaceutical

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 18
  • Latest Marketing Date 2026-01-05
  • Data Source FDA
  • First Marketing Date 1983-01-01
Company Overview

Company

Henan Lihua Pharmaceutical

Country

China

Social Profiles

Company Snapshot

Henan Lihua Pharmaceutical

Middle Of Huanghe Street,Anyang Hi-tech Industry Development Zone,Henan

China

en.hnlihua.com/ lihua@hnlihua.com View on Map
NDC Records ( 18 records )
2003
01 Jan
Bulk Ingredient NDC: 64958-0002

Nonproprietary Name

Prednisone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0002

Substance

PREDNISONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2004
09 Dec
Bulk Ingredient NDC: 64958-0012

Nonproprietary Name

Betamethasone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0012

Substance

BETAMETHASONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2004-12-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2007
06 Apr
Bulk Ingredient NDC: 64958-0020

Nonproprietary Name

Hydrocortisone Sodium Succinate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0020

Substance

HYDROCORTISONE SODIUM SUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2007-04-06

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1983
01 Jan
Bulk Ingredient NDC: 64958-0025

Nonproprietary Name

Cortisone Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0025

Substance

CORTISONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1983-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2006
03 Aug
Bulk Ingredient NDC: 64958-0030

Nonproprietary Name

Hydrocortisone butyrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0030

Substance

HYDROCORTISONE BUTYRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2006-08-03

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
01 Jan
Bulk Ingredient NDC: 64958-0034

Nonproprietary Name

Hydrocortisone Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0034

Substance

HYDROCORTISONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
01 Jan
Bulk Ingredient NDC: 64958-0036

Nonproprietary Name

Hydrocortisone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0036

Substance

HYDROCORTISONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
01 Jan
Bulk Ingredient NDC: 64958-0042

Nonproprietary Name

Prednisolone Sodium Phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0042

Substance

PREDNISOLONE SODIUM PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
01 Jan
Bulk Ingredient NDC: 64958-0048

Nonproprietary Name

Prednisolone Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0048

Substance

PREDNISOLONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
01 Jan
Bulk Ingredient NDC: 64958-0052

Nonproprietary Name

Prednisone Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0052

Substance

PREDNISONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2003
01 Jan
Bulk Ingredient NDC: 64958-0062

Nonproprietary Name

Hydrocortisone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0062

Substance

HYDROCORTISONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
26 Feb
Bulk Ingredient NDC: 64958-0063

Nonproprietary Name

Hydrocortisone Acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0063

Substance

HYDROCORTISONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-02-26

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
13 Dec
Bulk Ingredient NDC: 64958-0102

Nonproprietary Name

Trilostane

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0102

Substance

TRILOSTANE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-12-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
31 Mar
Bulk Ingredient NDC: 64958-0103

Nonproprietary Name

SPIRONOLACTONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0103

Substance

SPIRONOLACTONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-03-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
07 Jul
Bulk Ingredient NDC: 64958-0104

Nonproprietary Name

Budesonide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0104

Substance

BUDESONIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
27 Jul
Bulk Ingredient NDC: 64958-0105

Nonproprietary Name

Methylprednisolone acetate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0105

Substance

METHYLPREDNISOLONE ACETATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
27 Jul
Bulk Ingredient NDC: 64958-0106

Nonproprietary Name

Mometasone furoate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0106

Substance

MOMETASONE FUROATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-27

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
05 Jan
Bulk Ingredient NDC: 64958-0109

Nonproprietary Name

Prednisolone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Henan Lihua Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

64958-0109

Substance

PREDNISOLONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-01-05

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
18 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

64958-0002

Nonproprietary Name

Prednisone

Labeler

Henan Lihua Pharmaceutical Co Ltd

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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