Reyoung pharmaceutical
FDA Approved Drugs

Reyoung pharmaceutical

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 14
  • Latest Approval Date Mar 02, 2023
  • Data Source FDA
  • First Approval Date Mar 04, 2009
Company Overview

Company

Reyoung pharmaceutical

Country

China

Website

Visit Website

Email

wuguodong@reyoung.com

Social Profiles

LinkedIn
Company Snapshot

Reyoung pharmaceutical

No. 6 Erlangshan Road, Yi Yuan County, Shandong, PRC, 256100

China

www.reyoung.cn/en/ wuguodong@reyoung.com View on Map
FDA Approved Drug Records ( 14 records )
2017
16 Nov
RX Application: 207805

Drug Name

FENOFIBRATE (MICRONIZED)

Product Number

1

Dosage Form

-

Strength

67MG

Approval Date

2017-11-16

207805 / 1

Active Ingredient

FENOFIBRATE

Application Number

207805

Product Number

1

Dosage Form

-

Strength

67MG

Approval Date

2017-11-16

Regulatory Status

RX

2017
16 Nov
RX Application: 207805

Drug Name

FENOFIBRATE (MICRONIZED)

Product Number

2

Dosage Form

-

Strength

134MG

Approval Date

2017-11-16

207805 / 2

Active Ingredient

FENOFIBRATE

Application Number

207805

Product Number

2

Dosage Form

-

Strength

134MG

Approval Date

2017-11-16

Regulatory Status

RX

2017
16 Nov
RX Application: 207805

Drug Name

FENOFIBRATE (MICRONIZED)

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2017-11-16

207805 / 3

Active Ingredient

FENOFIBRATE

Application Number

207805

Product Number

3

Dosage Form

-

Strength

200MG

Approval Date

2017-11-16

Regulatory Status

RX

2021
17 Dec
RX Application: 212917

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2021-12-17

212917 / 1

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

212917

Product Number

1

Dosage Form

-

Strength

EQ 2.5MG BASE

Approval Date

2021-12-17

Regulatory Status

RX

2021
17 Dec
RX Application: 212917

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2021-12-17

212917 / 2

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

212917

Product Number

2

Dosage Form

-

Strength

EQ 5MG BASE

Approval Date

2021-12-17

Regulatory Status

RX

2021
17 Dec
RX Application: 212917

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2021-12-17

212917 / 3

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

212917

Product Number

3

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2021-12-17

Regulatory Status

RX

2021
17 Dec
RX Application: 212917

Drug Name

NEBIVOLOL HYDROCHLORIDE

Product Number

4

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2021-12-17

212917 / 4

Active Ingredient

NEBIVOLOL HYDROCHLORIDE

Application Number

212917

Product Number

4

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2021-12-17

Regulatory Status

RX

2009
04 Mar
RX Application: 78677

Drug Name

SERTRALINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2009-03-04

78677 / 1

Active Ingredient

SERTRALINE HYDROCHLORIDE

Application Number

78677

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2009-03-04

Regulatory Status

RX

2009
04 Mar
RX Application: 78677

Drug Name

SERTRALINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2009-03-04

78677 / 2

Active Ingredient

SERTRALINE HYDROCHLORIDE

Application Number

78677

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2009-03-04

Regulatory Status

RX

2009
04 Mar
RX Application: 78677

Drug Name

SERTRALINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2009-03-04

78677 / 3

Active Ingredient

SERTRALINE HYDROCHLORIDE

Application Number

78677

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2009-03-04

Regulatory Status

RX

2020
12 Jun
RX Application: 208494

Drug Name

SILDENAFIL CITRATE

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2020-06-12

208494 / 1

Active Ingredient

SILDENAFIL CITRATE

Application Number

208494

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE

Approval Date

2020-06-12

Regulatory Status

RX

2020
12 Jun
RX Application: 208494

Drug Name

SILDENAFIL CITRATE

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2020-06-12

208494 / 2

Active Ingredient

SILDENAFIL CITRATE

Application Number

208494

Product Number

2

Dosage Form

-

Strength

EQ 50MG BASE

Approval Date

2020-06-12

Regulatory Status

RX

2020
12 Jun
RX Application: 208494

Drug Name

SILDENAFIL CITRATE

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2020-06-12

208494 / 3

Active Ingredient

SILDENAFIL CITRATE

Application Number

208494

Product Number

3

Dosage Form

-

Strength

EQ 100MG BASE

Approval Date

2020-06-12

Regulatory Status

RX

2023
02 Mar
RX Application: 211337

Drug Name

TENOFOVIR DISOPROXIL FUMARATE

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2023-03-02

211337 / 1

Active Ingredient

TENOFOVIR DISOPROXIL FUMARATE

Application Number

211337

Product Number

1

Dosage Form

-

Strength

300MG

Approval Date

2023-03-02

Regulatory Status

RX

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Drug Status Breakdown
14 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

FENOFIBRATE (MICRONIZED)

Application Number

207805

Product Number

1

Active Ingredient

FENOFIBRATE

Dosage Form

-

Strength

67MG

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized FDA drug records

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