Arevipharma
Japan Drug Master Files (JDMF)

Arevipharma

Japan DMF Database

Japan Drug Master Files (JDMF) registered with Japan's Pharmaceuticals and Medical Devices Agency (PMDA).

APIs
  • Total Records 3
  • Latest Registration 2025-01-09
  • Data Source PMDA
  • Last Updated 2025-01-09
Company Overview

Company

Arevipharma

Country

Germany

Website

Visit Website

Email

Kerstin.dreissig@arevipharma.com

Social Profiles

LinkedIn
Company Snapshot

Arevipharma

Meißner Str. 35 01445 Radebeul

Germany

www.arevipharma.com/ Kerstin.dreissig@arevipharma.com View on Map
JDMF Records Timeline (3 records)
2011
19 Jul
APIs 223MF10112

Product

Thresemide

Company

Arevipharma GmbH

MF Registration No.

223MF10112

Domestic Manager

Initial Registration

2011-07-19

Latest Registration

2025-01-09

Registered Address

Meissner Strasse 35 D-01445 Radebeul, Germany

Country

Identifiers

MF Registration No.: 223MF10112

2024
20 Nov
APIs 306MF10148

Product

Fentanyl Citrate

Company

Arevipharma GmbH

MF Registration No.

306MF10148

Domestic Manager

Initial Registration

2024-11-20

Latest Registration

2024-11-20

Registered Address

Meissner Strasse 35 D-01445 Radebeul, Germany

Country

Identifiers

MF Registration No.: 306MF10148

2019
05 Jul
APIs 301MF10029

Product

Bisoprolol fumarate

Company

Arevipharma GmbH

MF Registration No.

301MF10029

Domestic Manager

Initial Registration

2019-07-05

Latest Registration

2019-07-05

Registered Address

Meissner Strasse 35 D-01445 Radebeul, Germany

Country

Identifiers

MF Registration No.: 301MF10029

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Official Source

All data is sourced from publicly available Japanese pharmaceutical regulatory sources and PMDA related publications.

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Record Details Preview

Click "View Details" on any record above to expand full details inline.

Country

Identifiers

MF Registration No.: 223MF10112

100% Official Data

Compiled from official PMDA & Japanese regulatory sources

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Data updated regularly from official sources

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Japan DMF (JDMF) data is compiled from publicly available Japanese pharmaceutical regulatory sources and PMDA related publications.

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