Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1MALLADI DRUGS AND PHARMACEUTICALS LIMITED Renigunta IN
02 1CHIFENG ARKER PHARMACEUTICAL TECHNOLOGY CO., LTD. Chifeng CN
03 1DIVI'S LABORATORIES LIMITED Hyderabad IN
04 1DSM Nutritional Products Ltd. Kaiseraugst CH
05 1EXEMED PHARMACEUTICALS Vadodara IN
06 1HY-GRO CHEMICALS PHARMTEK PRIVATE LIMITED Secunderabad IN
07 1SOLARA ACTIVE PHARMA SCIENCES LIMITED Chennai IN
08 1SRINI PHARMACEUTICALS PRIVATE LIMITED Choutuppal IN
09 1WANBURY LIMITED Vashi, Navi Mumbai IN
10 1Wockhardt Limited Mumbai IN
11 2ZHEJIANG APELOA KANGYU PHARMACEUTICAL CO., LTD. Hengdian CN
01 12Dextromethorphan hydrobromide monohydrate
01 3China
02 8India
03 1U.S.A
01 10Valid
02 2Withdrawn by Holder
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : CEP 2018-133 - Rev 01
Status : Valid
Issue Date : 2024-06-28
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : R0-CEP 2019-218 - Rev 00
Status : Valid
Issue Date : 2021-04-30
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : R1-CEP 1999-103 - Rev 06
Status : Valid
Issue Date : 2018-07-20
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : CEP 2021-257 - Rev 00
Status : Valid
Issue Date : 2023-12-20
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : R1-CEP 2014-023 - Rev 00
Status : Valid
Issue Date : 2020-07-23
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : R1-CEP 2013-288 - Rev 00
Status : Valid
Issue Date : 2022-06-28
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : R0-CEP 2018-201 - Rev 00
Status : Valid
Issue Date : 2021-03-17
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : CEP 2022-268 - Rev 00
Status : Valid
Issue Date : 2024-09-03
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : R1-CEP 1998-053 - Rev 04
Status : Valid
Issue Date : 2017-03-21
Type : Chemical
Substance Number : 20
Dextromethorphan Hydrobromide Monohydrate
Certificate Number : R0-CEP 2021-026 - Rev 00
Status : Valid
Issue Date : 2022-01-05
Type : Chemical
Substance Number : 20
A Dextromethorphan polistirex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dextromethorphan polistirex, including repackagers and relabelers. The FDA regulates Dextromethorphan polistirex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dextromethorphan polistirex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Dextromethorphan polistirex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dextromethorphan polistirex supplier is an individual or a company that provides Dextromethorphan polistirex active pharmaceutical ingredient (API) or Dextromethorphan polistirex finished formulations upon request. The Dextromethorphan polistirex suppliers may include Dextromethorphan polistirex API manufacturers, exporters, distributors and traders.
click here to find a list of Dextromethorphan polistirex suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dextromethorphan polistirex CEP of the European Pharmacopoeia monograph is often referred to as a Dextromethorphan polistirex Certificate of Suitability (COS). The purpose of a Dextromethorphan polistirex CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Dextromethorphan polistirex EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Dextromethorphan polistirex to their clients by showing that a Dextromethorphan polistirex CEP has been issued for it. The manufacturer submits a Dextromethorphan polistirex CEP (COS) as part of the market authorization procedure, and it takes on the role of a Dextromethorphan polistirex CEP holder for the record. Additionally, the data presented in the Dextromethorphan polistirex CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Dextromethorphan polistirex DMF.
A Dextromethorphan polistirex CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Dextromethorphan polistirex CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Dextromethorphan polistirex suppliers with CEP (COS) on PharmaCompass.
We have 10 companies offering Dextromethorphan polistirex
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