01 1Nagaoka Jitsugyo Co., Ltd.
02 1Ogi Pharmaceutical Co., Ltd.
03 1Symrise AG
04 1Takasago International Corporation
05 2Toyo Mint Industry Co., Ltd.
01 2Japanese Pharmacopoeia l- menthol (production only)
02 1Menthol JP
03 2l- menthol
04 1l- menthol SL-21
01 1Germany
02 5Japan
Japanese Pharmacopoeia l-Menthol (for manufacturing purposes only)
Registration Number : 218MF10275
Registrant's Address : 2-5-8 Doshomachi, Chuo-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2006-02-23
Latest Date of Registration : 2006-02-23
Japanese Pharmacopoeia l-Menthol (for manufacturing purposes only)
Registration Number : 217MF10801
Registrant's Address : 4-7-18 Nishinomiyahama, Nishinomiya City, Hyogo Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2006-11-15
Registration Number : 218MF10705
Registrant's Address : Muehlenfeldstrasse 1 D-37 603 Holzminden Germany
Initial Date of Registration : 2006-08-11
Latest Date of Registration : 2013-05-09
Registration Number : 217MF11171
Registrant's Address : 5-37-1 Kamata, Ota-ku, Tokyo
Initial Date of Registration : 2005-12-12
Latest Date of Registration : 2010-04-01
Registration Number : 217MF10175
Registrant's Address : 75-1 Hamanaka, Satosho-cho, Asakuchi-gun, Okayama Prefecture
Initial Date of Registration : 2005-05-31
Latest Date of Registration : 2006-11-15
Registration Number : 217MF10179
Registrant's Address : 75-1 Hamanaka, Satosho-cho, Asakuchi-gun, Okayama Prefecture
Initial Date of Registration : 2005-05-31
Latest Date of Registration : 2007-03-14
53
PharmaCompass offers a list of Levomenthol API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levomenthol manufacturer or Levomenthol supplier for your needs.
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A Robitussin Cough Drops manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Robitussin Cough Drops, including repackagers and relabelers. The FDA regulates Robitussin Cough Drops manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Robitussin Cough Drops API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Robitussin Cough Drops supplier is an individual or a company that provides Robitussin Cough Drops active pharmaceutical ingredient (API) or Robitussin Cough Drops finished formulations upon request. The Robitussin Cough Drops suppliers may include Robitussin Cough Drops API manufacturers, exporters, distributors and traders.
click here to find a list of Robitussin Cough Drops suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Robitussin Cough Drops Drug Master File in Japan (Robitussin Cough Drops JDMF) empowers Robitussin Cough Drops API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Robitussin Cough Drops JDMF during the approval evaluation for pharmaceutical products. At the time of Robitussin Cough Drops JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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