Kao Corporation
Japan Drug Master Files (JDMF)

Kao Corporation

Japan DMF Database

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

APIs
  • Total Records 3
  • Latest Registration 2021-10-21
  • Data Source PMDA
  • Last Updated 2021-10-21
Company Overview

Company

Kao Corporation

Country

Japan

Email

Social Profiles

Company Snapshot

Kao Corporation

1-14-10, Nihonbashi Kayabacho, Tokyo, Kanto 103-8210, JP

Japan

www.kao.com/global/en/ View on Map
JDMF Records Timeline (3 records)
2005
18 May
APIs 217MF10005

Product

Sanizol L-80

Company

Kao Corporation

MF Registration No.

217MF10005

Domestic Manager

Initial Registration

2005-05-18

Latest Registration

2021-10-21

Registered Address

1-14-10 Nihonbashi Kayabacho, Chuo-ku, Tokyo

Country

Identifiers

MF Registration No.: 217MF10005

2010
25 Feb
APIs 222MF10072

Product

Japanese Pharmacopoeia Glycerin

Company

Kao Corporation

MF Registration No.

222MF10072

Domestic Manager

Initial Registration

2010-02-25

Latest Registration

2010-02-25

Registered Address

1-14-10 Nihonbashi Kayabacho, Chuo-ku, Tokyo

Country

Identifiers

MF Registration No.: 222MF10072

2005
18 May
APIs 217MF10004

Product

Sanizol C

Company

Kao Corporation

MF Registration No.

217MF10004

Domestic Manager

Initial Registration

2005-05-18

Latest Registration

2007-07-02

Registered Address

1-14-10 Nihonbashi Kayabacho, Chuo-ku, Tokyo

Country

Identifiers

MF Registration No.: 217MF10004

Related Databases
  • FDA Inspections
    0 View
  • EDQM CEP
    0 View
  • KDMF
    0 View
  • Japan DMF
    3 View
  • Eudra GMP
    0 View
Category Breakdown
3 total
  • APIs
Official Source

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

Visit PMDA
Record Details Preview

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

Country

Identifiers

MF Registration No.: 217MF10005

100% Official Data

Compiled from official PMDA & Japanese regulatory sources

Regular Updates

Data updated regularly from official sources

Trusted by Professionals

100K+ pharma professionals worldwide

Secure & Reliable

Enterprise-grade security and data protection

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

Create a New Buying Request

Fields marked with * are mandatory.

Please enter quantity.
Please select a unit.
Please select quality standard.
Please select request type.
Please provide product specifications.
Please enter additional details.
Please select shipping preference.
Notice: By submitting this buying request, the provided product details and requirements may be published publicly on our marketplace.