HEC Pharm
FDA Approved Drugs

HEC Pharm

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.

RX Discontinued
  • Total Records 14
  • Latest Approval Date Feb 05, 2019
  • Data Source FDA
  • First Approval Date Oct 07, 2011
All
14
View
Discontinued
3
View
RX
11
View
Company Overview

Company

HEC Pharm

Country

China

Website

Visit Website

Email

sales@hecpharm.com

Social Profiles

Company Snapshot

HEC Pharm

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 ( 14 records )
2015
28 Sep
RX Application: 203584

Drug Name

CLARITHROMYCIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2015-09-28

203584 / 1

Active Ingredient

CLARITHROMYCIN

Application Number

203584

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2015-09-28

Regulatory Status

RX

2015
28 Sep
RX Application: 203584

Drug Name

CLARITHROMYCIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2015-09-28

203584 / 2

Active Ingredient

CLARITHROMYCIN

Application Number

203584

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2015-09-28

Regulatory Status

RX

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

2019
05 Feb
RX Application: 204968

Drug Name

LEVOFLOXACIN

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2019-02-05

204968 / 1

Active Ingredient

LEVOFLOXACIN

Application Number

204968

Product Number

1

Dosage Form

-

Strength

250MG

Approval Date

2019-02-05

Regulatory Status

RX

2019
05 Feb
RX Application: 204968

Drug Name

LEVOFLOXACIN

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2019-02-05

204968 / 2

Active Ingredient

LEVOFLOXACIN

Application Number

204968

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

2019-02-05

Regulatory Status

RX

2019
05 Feb
RX Application: 204968

Drug Name

LEVOFLOXACIN

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

2019-02-05

204968 / 3

Active Ingredient

LEVOFLOXACIN

Application Number

204968

Product Number

3

Dosage Form

-

Strength

750MG

Approval Date

2019-02-05

Regulatory Status

RX

2018
02 Jul
RX Application: 208146

Drug Name

OLANZAPINE

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2018-07-02

208146 / 1

Active Ingredient

OLANZAPINE

Application Number

208146

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2018-07-02

Regulatory Status

RX

2018
02 Jul
RX Application: 208146

Drug Name

OLANZAPINE

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2018-07-02

208146 / 2

Active Ingredient

OLANZAPINE

Application Number

208146

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2018-07-02

Regulatory Status

RX

2018
02 Jul
RX Application: 208146

Drug Name

OLANZAPINE

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2018-07-02

208146 / 3

Active Ingredient

OLANZAPINE

Application Number

208146

Product Number

3

Dosage Form

-

Strength

15MG

Approval Date

2018-07-02

Regulatory Status

RX

2018
02 Jul
RX Application: 208146

Drug Name

OLANZAPINE

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2018-07-02

208146 / 4

Active Ingredient

OLANZAPINE

Application Number

208146

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

2018-07-02

Regulatory Status

RX

2019
16 Jan
RX Application: 206021

Drug Name

PRASUGREL

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2019-01-16

206021 / 1

Active Ingredient

PRASUGREL HYDROCHLORIDE

Application Number

206021

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2019-01-16

Regulatory Status

RX

2019
16 Jan
RX Application: 206021

Drug Name

PRASUGREL

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2019-01-16

206021 / 2

Active Ingredient

PRASUGREL HYDROCHLORIDE

Application Number

206021

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2019-01-16

Regulatory Status

RX

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
14 total
  • RX
  • 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

CLARITHROMYCIN

Application Number

203584

Product Number

1

Active Ingredient

CLARITHROMYCIN

Dosage Form

-

Strength

250MG

FDA Approved Drug Data

Approved drug product information

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