Mundipharma
FDA Approved Drugs

Mundipharma

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 1
  • Latest Approval Date Mar 22, 2023
  • Data Source FDA
  • First Approval Date Mar 22, 2023
Company Overview

Company

Mundipharma

Country

Germany

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Company Snapshot

Mundipharma

Höhenstraße 10 65549 Limburg Germany

Germany

www.mundipharmaresearch.com/ info@mundipharma-rd.eu View on Map
FDA Approved Drug Records ( 1 record )
2023
22 Mar
RX Application: 217417

Drug Name

REZZAYO

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/VIAL

Approval Date

2023-03-22

217417 / 1

Active Ingredient

REZAFUNGIN ACETATE

Application Number

217417

Product Number

1

Dosage Form

-

Strength

EQ 200MG BASE/VIAL

Approval Date

2023-03-22

Regulatory Status

RX

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Drug Status Breakdown
1 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

REZZAYO

Application Number

217417

Product Number

1

Active Ingredient

REZAFUNGIN ACETATE

Dosage Form

-

Strength

EQ 200MG BASE/VIAL

FDA Approved Drug Data

Approved drug product information

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