HEC Pharm Discontinued
FDA Approved Drugs

HEC Pharm Discontinued

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

Discontinued
  • Total Records 3
  • Latest Approval Date May 18, 2018
  • Data Source FDA
  • First Approval Date Oct 07, 2011
All
14
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Discontinued
3
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RX
11
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Company Overview

Company

HEC Pharm Discontinued

Country

China

Social Profiles

Company Snapshot

HEC Pharm Discontinued

Dong Yang Guang Park, Zhenan Road No.368, Shang Sha Village, Changan Town, Dongguan, Guangdong, Chi

China

www.hecpharm.com/ sales@hecpharm.com View on Map
FDA Approved Drug Records ( 3 records )
2018
18 May
Discontinued Application: 207265

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2018-05-18

207265 / 1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

207265

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2018-05-18

Regulatory Status

Discontinued

2018
18 May
Discontinued Application: 207265

Drug Name

ESOMEPRAZOLE MAGNESIUM

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2018-05-18

207265 / 2

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Application Number

207265

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2018-05-18

Regulatory Status

Discontinued

2011
07 Oct
Discontinued Application: 202058

Drug Name

ZIDOVUDINE

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2011-10-07

202058 / 1

Active Ingredient

ZIDOVUDINE

Application Number

202058

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2011-10-07

Regulatory Status

Discontinued

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Drug Status Breakdown
3 total
  • Discontinued
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

ESOMEPRAZOLE MAGNESIUM

Application Number

207265

Product Number

1

Active Ingredient

ESOMEPRAZOLE MAGNESIUM

Dosage Form

-

Strength

EQ 40MG BASE

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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Searchable pharmaceutical data

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