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01 1SWATI SPENTOSE PRIVATE LIMITED Mumbai IN
02 1COHANCE LIFESCIENCES LIMITED Hyderabad IN
03 1APITORIA PHARMA PRIVATE LIMITED Hyderabad IN
04 1ASTELLAS PHARMA INC. Tokyo JP
05 1BIOINDUSTRIA L.I.M. S.P.A. Novi Ligure IT
06 2CIPLA LIMITED Mumbai IN
07 1DONG BANG FUTURE TECH & LIFE CO., LTD. Hwaseong-si KR
08 1MACLEODS PHARMACEUTICALS LIMITED Mumbai IN
09 1QUIMICA SINTETICA S.A. Alcala De Henares ES
10 1SCINOPHARM TAIWAN, LTD. Shan-Hua TW
11 1SUN PHARMACEUTICAL INDUSTRIES LIMITED Mumbai IN
12 1SUVEN PHARMACEUTICALS LIMITED Hyderabad IN
13 1SYNTHON BV Nijmegen NL
14 1TYCHE INDUSTRIES LIMITED Hyderabad IN
15 1UNICHEM LABORATORIES LIMITED Mumbai IN
16 1VASUDHA PHARMA CHEM LIMITED Hyderabad IN
17 1Wockhardt Limited Mumbai IN
18 1ZENTIVA K.S. Prague CZ
19 1ZENTIVA K.S. Praha 10 CZ
20 1ZYDUS LIFESCIENCES LIMITED Vadodara IN
SWATI – Transforming science into solutions with 50+ years of expertise, global accreditations, and pioneering biotech innovation.
Certificate Number : CEP 2022-133 - Rev 02
Status : Valid
Issue Date : 2025-07-29
Type : Chemical
Substance Number : 2131
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Certificate Number : R1-CEP 2012-309 - Rev 02
Status : Valid
Issue Date : 2022-12-15
Type : Chemical
Substance Number : 2131
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PharmaCompass offers a list of Tamsulosin 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 Tamsulosin manufacturer or Tamsulosin supplier for your needs.
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A 106138-88-9 (Parent) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 106138-88-9 (Parent), including repackagers and relabelers. The FDA regulates 106138-88-9 (Parent) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 106138-88-9 (Parent) 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 106138-88-9 (Parent) supplier is an individual or a company that provides 106138-88-9 (Parent) active pharmaceutical ingredient (API) or 106138-88-9 (Parent) finished formulations upon request. The 106138-88-9 (Parent) suppliers may include 106138-88-9 (Parent) API manufacturers, exporters, distributors and traders.
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A 106138-88-9 (Parent) CEP of the European Pharmacopoeia monograph is often referred to as a 106138-88-9 (Parent) Certificate of Suitability (COS). The purpose of a 106138-88-9 (Parent) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 106138-88-9 (Parent) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 106138-88-9 (Parent) to their clients by showing that a 106138-88-9 (Parent) CEP has been issued for it. The manufacturer submits a 106138-88-9 (Parent) CEP (COS) as part of the market authorization procedure, and it takes on the role of a 106138-88-9 (Parent) CEP holder for the record. Additionally, the data presented in the 106138-88-9 (Parent) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 106138-88-9 (Parent) DMF.
A 106138-88-9 (Parent) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 106138-88-9 (Parent) 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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We have 19 companies offering 106138-88-9 (Parent)
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