Yaopharma Co., Ltd. Discontinued
FDA Approved Drugs

Yaopharma Co., Ltd. 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 5
  • Latest Approval Date Nov 04, 2019
  • Data Source FDA
  • First Approval Date Aug 16, 2019
All
12
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Discontinued
5
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RX
7
View
Company Overview

Company

Yaopharma Co., Ltd. Discontinued

Country

China

Website

Visit Website

Email

carolyn.wang@yaopharma.com

Social Profiles

Company Snapshot

Yaopharma Co., Ltd. Discontinued

100 Xingguang Avenue, Renhe Town, Yubei District

China

www.yaopharma.com/ carolyn.wang@yaopharma.com View on Map
FDA Approved Drug Records ( 5 records )
2019
16 Aug
Discontinued Application: 207219

Drug Name

DULOXETINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2019-08-16

207219 / 1

Active Ingredient

DULOXETINE HYDROCHLORIDE

Application Number

207219

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2019-08-16

Regulatory Status

Discontinued

2019
16 Aug
Discontinued Application: 207219

Drug Name

DULOXETINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2019-08-16

207219 / 2

Active Ingredient

DULOXETINE HYDROCHLORIDE

Application Number

207219

Product Number

2

Dosage Form

-

Strength

EQ 30MG BASE

Approval Date

2019-08-16

Regulatory Status

Discontinued

2019
16 Aug
Discontinued Application: 207219

Drug Name

DULOXETINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 60MG BASE

Approval Date

2019-08-16

207219 / 3

Active Ingredient

DULOXETINE HYDROCHLORIDE

Application Number

207219

Product Number

3

Dosage Form

-

Strength

EQ 60MG BASE

Approval Date

2019-08-16

Regulatory Status

Discontinued

2019
04 Nov
Discontinued Application: 212201

Drug Name

ENTECAVIR

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2019-11-04

212201 / 1

Active Ingredient

ENTECAVIR

Application Number

212201

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2019-11-04

Regulatory Status

Discontinued

2019
04 Nov
Discontinued Application: 212201

Drug Name

ENTECAVIR

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2019-11-04

212201 / 2

Active Ingredient

ENTECAVIR

Application Number

212201

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2019-11-04

Regulatory Status

Discontinued

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Drug Status Breakdown
5 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

DULOXETINE HYDROCHLORIDE

Application Number

207219

Product Number

1

Active Ingredient

DULOXETINE HYDROCHLORIDE

Dosage Form

-

Strength

EQ 20MG BASE

FDA Approved Drug Data

Approved drug product information

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Data maintained from official sources

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