Yaopharma Co., Ltd. RX
FDA Approved Drugs

Yaopharma Co., Ltd. RX

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
  • Total Records 7
  • Latest Approval Date Jun 09, 2026
  • Data Source FDA
  • First Approval Date May 28, 2015
All
12
View
Discontinued
5
View
RX
7
View
Company Overview

Company

Yaopharma Co., Ltd. RX

Country

China

Social Profiles

Company Snapshot

Yaopharma Co., Ltd. RX

100 Xingguang Avenue, Renhe Town, Yubei District

China

www.yaopharma.com/ carolyn.wang@yaopharma.com View on Map
FDA Approved Drug Records ( 7 records )
2026
09 Jun
RX Application: 215552

Drug Name

TOFACITINIB CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2026-06-09

215552 / 1

Active Ingredient

TOFACITINIB CITRATE

Application Number

215552

Product Number

1

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2026-06-09

Regulatory Status

RX

2026
09 Jun
RX Application: 215552

Drug Name

TOFACITINIB CITRATE

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2026-06-09

215552 / 2

Active Ingredient

TOFACITINIB CITRATE

Application Number

215552

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2026-06-09

Regulatory Status

RX

2015
28 May
RX Application: 202036

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2015-05-28

202036 / 1

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

202036

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2015-05-28

Regulatory Status

RX

2015
28 May
RX Application: 202036

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2015-05-28

202036 / 2

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

202036

Product Number

2

Dosage Form

-

Strength

EQ 37.5MG BASE

Approval Date

2015-05-28

Regulatory Status

RX

2015
28 May
RX Application: 202036

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2015-05-28

202036 / 3

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

202036

Product Number

3

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2015-05-28

Regulatory Status

RX

2015
28 May
RX Application: 202036

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2015-05-28

202036 / 4

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

202036

Product Number

4

Dosage Form

-

Strength

EQ 75MG BASE

Approval Date

2015-05-28

Regulatory Status

RX

2015
28 May
RX Application: 202036

Drug Name

VENLAFAXINE HYDROCHLORIDE

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2015-05-28

202036 / 5

Active Ingredient

VENLAFAXINE HYDROCHLORIDE

Application Number

202036

Product Number

5

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2015-05-28

Regulatory Status

RX

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Drug Status Breakdown
7 total
  • RX
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

TOFACITINIB CITRATE

Application Number

215552

Product Number

1

Active Ingredient

TOFACITINIB CITRATE

Dosage Form

-

Strength

EQ 5MG BASE

FDA Approved Drug Data

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