Hubei Haosun Pharmaceutical Co., Ltd.
NDC Database

Hubei Haosun Pharmaceutical 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
  • Total Records 11
  • Latest Marketing Date 2025-05-14
  • Data Source FDA
  • First Marketing Date 2011-10-10
Company Overview

Company

Hubei Haosun Pharmaceutical Co., Ltd.

Country

China

Website

Visit Website

Email

haosun@haosun.com

Social Profiles

Company Snapshot

Hubei Haosun Pharmaceutical Co., Ltd.

Add:No.20 Juxian Road, Gedian Economical DevelopmentZone, Hubei Province,

China

www.haosun.com.cn/ haosun@haosun.com View on Map
NDC Records ( 11 records )
2011
10 Oct
Bulk Ingredient NDC: 14778-0101

Nonproprietary Name

FLUMAZENIL

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-0101

Substance

FLUMAZENIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Oct
Bulk Ingredient NDC: 14778-0202

Nonproprietary Name

Granisetron

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-0202

Substance

GRANISETRON

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Oct
Bulk Ingredient NDC: 14778-0303

Nonproprietary Name

Granisetron Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-0303

Substance

GRANISETRON HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
28 Jun
Bulk Ingredient NDC: 14778-0505

Nonproprietary Name

DASATINIB ANHYDROUS

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-0505

Substance

DASATINIB ANHYDROUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-06-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2021
23 Jun
Bulk Ingredient NDC: 14778-0606

Nonproprietary Name

DESVENLAFAXINE SUCCINATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-0606

Substance

DESVENLAFAXINE SUCCINATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2021-06-23

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
11 Jan
Bulk Ingredient NDC: 14778-0707

Nonproprietary Name

NEOSTIGMINE METHYLSULFATE

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-0707

Substance

NEOSTIGMINE METHYLSULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-01-11

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
14 May
Bulk Ingredient NDC: 14778-0808

Nonproprietary Name

NILOTINIB HYDROCHLORIDE MONOHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-0808

Substance

NILOTINIB HYDROCHLORIDE MONOHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-05-14

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Oct
Bulk Ingredient NDC: 14778-1111

Nonproprietary Name

Irinotecan Hydrochloride

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-1111

Substance

IRINOTECAN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Oct
Bulk Ingredient NDC: 14778-1212

Nonproprietary Name

Docetaxel Anhydrous

Dosage Form

POWDER

Strength

1 g/g

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-1212

Substance

DOCETAXEL ANHYDROUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Oct
Bulk Ingredient NDC: 14778-1313

Nonproprietary Name

Dasatinib

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-1313

Substance

DASATINIB

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Oct
Bulk Ingredient NDC: 14778-1414

Nonproprietary Name

Temozolomide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Hubei Haosun Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

14778-1414

Substance

TEMOZOLOMIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-10-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
11 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

14778-0101

Nonproprietary Name

FLUMAZENIL

Labeler

Hubei Haosun 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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