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01 1ZAKŁADY FARMACEUTYCZNE POLPHARMA S.A. Starogard Gdański PL

02 1DR. REDDY'S LABORATORIES LIMITED Hyderabad IN

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13 1Cambrex Profarmaco Milano S.r.l. Paullo IT

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PharmaCompass
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

CEP 2021-270 - Rev 03
Valid
Chemical
2024-08-23
2932
Polpharma CB

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothPolpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

Rivaroxaban, Non-micronised, Micronised

Certificate Number : CEP 2021-270 - Rev 03

Status : Valid

Issue Date : 2024-08-23

Type : Chemical

Substance Number : 2932

Polpharma CB
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

R0-CEP 2020-250 - Rev 01
Valid
Chemical
2022-10-14
2932
Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Rivaroxaban

Certificate Number : R0-CEP 2020-250 - Rev 01

Status : Valid

Issue Date : 2022-10-14

Type : Chemical

Substance Number : 2932

Dr Reddy Company Banner
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

CEP 2020-274 - Rev 02
Valid
Chemical
2024-06-28
2932
Cohance

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

Rivaroxaban

Certificate Number : CEP 2020-274 - Rev 02

Status : Valid

Issue Date : 2024-06-28

Type : Chemical

Substance Number : 2932

Cohance
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAMI Lifesciences is Driven by Chemistry. Powered by People.

CEP 2022-215 - Rev 01
Valid
Chemical
2025-03-12
2932
AMI Lifesciences

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAMI Lifesciences is Driven by Chemistry. Powered by People.

Rivaroxaban

Certificate Number : CEP 2022-215 - Rev 01

Status : Valid

Issue Date : 2025-03-12

Type : Chemical

Substance Number : 2932

AMI Lifesciences

Looking for 366789-02-8 / Rivaroxaban API manufacturers, exporters & distributors?

Rivaroxaban manufacturers, exporters & distributors 1

79

PharmaCompass offers a list of Rivaroxaban 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 Rivaroxaban manufacturer or Rivaroxaban supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rivaroxaban manufacturer or Rivaroxaban supplier.

PharmaCompass also assists you with knowing the Rivaroxaban API Price utilized in the formulation of products. Rivaroxaban API Price is not always fixed or binding as the Rivaroxaban Price is obtained through a variety of data sources. The Rivaroxaban Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Rivaroxaban

Synonyms

366789-02-8, Xarelto, Bay 59-7939, (s)-5-chloro-n-((2-oxo-3-(4-(3-oxomorpholino)phenyl)oxazolidin-5-yl)methyl)thiophene-2-carboxamide, Bay59-7939, Bay-59-7939

Cas Number

366789-02-8

Unique Ingredient Identifier (UNII)

9NDF7JZ4M3

About Rivaroxaban

A morpholine and thiophene derivative that functions as a FACTOR XA INHIBITOR and is used in the treatment and prevention of DEEP-VEIN THROMBOSIS and PULMONARY EMBOLISM. It is also used for the prevention of STROKE and systemic embolization in patients with non-valvular ATRIAL FIBRILLATION, and for the prevention of atherothrombotic events in patients after an ACUTE CORONARY SYNDROME.

RIV Manufacturers

A RIV manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RIV, including repackagers and relabelers. The FDA regulates RIV manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RIV 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 RIV manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

RIV Suppliers

A RIV supplier is an individual or a company that provides RIV active pharmaceutical ingredient (API) or RIV finished formulations upon request. The RIV suppliers may include RIV API manufacturers, exporters, distributors and traders.

click here to find a list of RIV suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

RIV CEP

A RIV CEP of the European Pharmacopoeia monograph is often referred to as a RIV Certificate of Suitability (COS). The purpose of a RIV CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of RIV EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of RIV to their clients by showing that a RIV CEP has been issued for it. The manufacturer submits a RIV CEP (COS) as part of the market authorization procedure, and it takes on the role of a RIV CEP holder for the record. Additionally, the data presented in the RIV CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the RIV DMF.

A RIV CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. RIV 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 RIV suppliers with CEP (COS) on PharmaCompass.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.