Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
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01 1Vamsi Labs Limited Solapur IN
02 1AARTI PHARMALABS LIMITED Mulund (W), Mumbai IN
03 1NEULAND LABORATORIES LIMITED Hyderabad IN
04 1Boehringer Ingelheim Pharma GmbH & Co. KG Ingelheim Am Rhein DE
05 1CIPLA LIMITED Mumbai IN
06 1Lusochimica S.p.A. Lomagna IT
07 1MELODY HEALTHCARE PVT. LTD. Mumbai IN
08 1OLON S.P.A. Rodano IT
09 1SCL LIFESCIENCES LIMITED Sahibzada Ajit Singh Nagar IN
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01 8Ipratropium bromide
02 1Ipratropium bromide, Micronised
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01 1Germany
02 5India
03 2Italy
04 1Blank
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01 8Valid
02 1Withdrawn by Holder
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
Ipratropium Bromide, Micronised
Certificate Number : CEP 2023-137 - Rev 00
Status : Valid
Issue Date : 2024-11-05
Type : Chemical
Substance Number : 919
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Certificate Number : R1-CEP 2008-150 - Rev 03
Status : Valid
Issue Date : 2022-10-14
Type : Chemical
Substance Number : 919
Certificate Number : R1-CEP 2012-126 - Rev 02
Status : Valid
Issue Date : 2023-04-14
Type : Chemical
Substance Number : 919
Certificate Number : R1-CEP 1996-005 - Rev 05
Status : Valid
Issue Date : 2015-10-08
Type : Chemical
Substance Number : 919
Certificate Number : R0-CEP 2015-340 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2016-12-16
Type : Chemical
Substance Number : 919
Certificate Number : R1-CEP 2004-220 - Rev 01
Status : Valid
Issue Date : 2020-11-26
Type : Chemical
Substance Number : 919
Certificate Number : CEP 2017-302 - Rev 03
Status : Valid
Issue Date : 2024-04-15
Type : Chemical
Substance Number : 919
Certificate Number : R1-CEP 1998-083 - Rev 08
Status : Valid
Issue Date : 2021-06-28
Type : Chemical
Substance Number : 919
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : CEP 2022-470 - Rev 01
Status : Valid
Issue Date : 2025-03-17
Type : Chemical
Substance Number : 919
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Ipratropium Bromide 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 Ipratropium Bromide manufacturer or Ipratropium Bromide supplier for your needs.
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PharmaCompass also assists you with knowing the Ipratropium Bromide API Price utilized in the formulation of products. Ipratropium Bromide API Price is not always fixed or binding as the Ipratropium Bromide Price is obtained through a variety of data sources. The Ipratropium Bromide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A COMBIVENT-1 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of COMBIVENT-1, including repackagers and relabelers. The FDA regulates COMBIVENT-1 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. COMBIVENT-1 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 COMBIVENT-1 supplier is an individual or a company that provides COMBIVENT-1 active pharmaceutical ingredient (API) or COMBIVENT-1 finished formulations upon request. The COMBIVENT-1 suppliers may include COMBIVENT-1 API manufacturers, exporters, distributors and traders.
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A COMBIVENT-1 CEP of the European Pharmacopoeia monograph is often referred to as a COMBIVENT-1 Certificate of Suitability (COS). The purpose of a COMBIVENT-1 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of COMBIVENT-1 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of COMBIVENT-1 to their clients by showing that a COMBIVENT-1 CEP has been issued for it. The manufacturer submits a COMBIVENT-1 CEP (COS) as part of the market authorization procedure, and it takes on the role of a COMBIVENT-1 CEP holder for the record. Additionally, the data presented in the COMBIVENT-1 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the COMBIVENT-1 DMF.
A COMBIVENT-1 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. COMBIVENT-1 CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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