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PharmaCompass

01

Peptide Therapy Summit
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothInterquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

GDUFA

DMF Review : Complete

Rev. Date : 2015-01-05

Pay. Date : 2014-07-23

DMF Number : 28471

Submission : 2014-07-31

Status : Active

Type : II

Interquim

02

Peptide Therapy Summit
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothVeranova: A CDMO that manages complexity with confidence.

GDUFA

DMF Review : Complete

Rev. Date : 2018-02-28

Pay. Date : 2017-09-25

DMF Number : 32093

Submission : 2017-10-31

Status : Active

Type : II

Veranova

03

Peptide Therapy Summit
Not Confirmed

04

Peptide Therapy Summit
Not Confirmed

06

Peptide Therapy Summit
Not Confirmed

06

08

Peptide Therapy Summit
Not Confirmed

09

Peptide Therapy Summit
Not Confirmed

10

Peptide Therapy Summit
Not Confirmed

Looking for 162401-32-3 / Roflumilast API manufacturers, exporters & distributors?

Roflumilast manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Roflumilast

Synonyms

162401-32-3, Daxas, 3-(cyclopropylmethoxy)-n-(3,5-dichloropyridin-4-yl)-4-(difluoromethoxy)benzamide, Daliresp, By217, Byk20869

Cas Number

162401-32-3

Unique Ingredient Identifier (UNII)

0P6C6ZOP5U

About Roflumilast

Roflumilast is an orally available, long-acting inhibitor of phosphodiesterase (PDE) type 4 (PDE4), with anti-inflammatory and potential antineoplastic activities. Upon administration, roflumilast and its active metabolite roflumilast N-oxide selectively and competitively bind to and inhibit PDE4, which leads to an increase of both intracellular levels of cyclic-3',5'-adenosine monophosphate (cAMP) and cAMP-mediated signaling. cAMP prevents phosphorylation of spleen tyrosine kinase (SYK) and abrogates activation of the PI3K/AKT/mTOR signaling pathway, which may result in the induction of apoptosis. PDE4, a member of the PDE superfamily that hydrolyses cAMP and 3',5'-cyclic guanosine monophosphate (cGMP) to their inactive 5' monophosphates, is upregulated in a variety of cancers and may contribute to chemoresistance; it also plays a key role in inflammation, especially in inflammatory airway diseases.

BY217 Manufacturers

A BY217 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BY217, including repackagers and relabelers. The FDA regulates BY217 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BY217 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 BY217 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

BY217 Suppliers

A BY217 supplier is an individual or a company that provides BY217 active pharmaceutical ingredient (API) or BY217 finished formulations upon request. The BY217 suppliers may include BY217 API manufacturers, exporters, distributors and traders.

click here to find a list of BY217 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

BY217 USDMF

A BY217 DMF (Drug Master File) is a document detailing the whole manufacturing process of BY217 active pharmaceutical ingredient (API) in detail. Different forms of BY217 DMFs exist exist since differing nations have different regulations, such as BY217 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A BY217 DMF submitted to regulatory agencies in the US is known as a USDMF. BY217 USDMF includes data on BY217's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The BY217 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of BY217 suppliers with USDMF on PharmaCompass.

BY217 Manufacturers | Traders | Suppliers

BY217 Manufacturers, Traders, Suppliers 1
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.