Shionogi RX
FDA Approved Drugs

Shionogi 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 3
  • Latest Approval Date May 29, 2026
  • Data Source FDA
  • First Approval Date Nov 14, 2019
All
11
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Discontinued
8
View
RX
3
View
Company Overview

Company

Shionogi RX

Country

Japan

Email

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Company Snapshot

Shionogi RX

1-8, Doshomachi 3-chome, Chuo-ku, Osaka 541-0045

Japan

www.shionogi.com/eu/en/ View on Map
FDA Approved Drug Records ( 3 records )
2019
14 Nov
RX Application: 209445

Drug Name

FETROJA

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2019-11-14

209445 / 1

Active Ingredient

CEFIDEROCOL SULFATE TOSYLATE

Application Number

209445

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2019-11-14

Regulatory Status

RX

2022
12 May
RX Application: 215446

Drug Name

RADICAVA ORS

Product Number

1

Dosage Form

-

Strength

105MG/5ML

Approval Date

2022-05-12

215446 / 1

Active Ingredient

EDARAVONE

Application Number

215446

Product Number

1

Dosage Form

-

Strength

105MG/5ML

Approval Date

2022-05-12

Regulatory Status

RX

2026
29 May
RX Application: 220442

Drug Name

XOCOVA

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

2026-05-29

220442 / 1

Active Ingredient

ENSITRELVIR

Application Number

220442

Product Number

1

Dosage Form

-

Strength

125MG

Approval Date

2026-05-29

Regulatory Status

RX

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Drug Status Breakdown
3 total
  • RX
Official Source

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

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FDA Approved Drug Record Details Preview

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

Drug Name

FETROJA

Application Number

209445

Product Number

1

Active Ingredient

CEFIDEROCOL SULFATE TOSYLATE

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

FDA Approved Drug Data

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