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Looking for 39562-70-4 / Nitrendipine API manufacturers, exporters & distributors?

Nitrendipine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Nitrendipine

Synonyms

39562-70-4, Bayotensin, Baypress, Nidrel, Deiten, Bay-e-5009

Cas Number

39562-70-4

Unique Ingredient Identifier (UNII)

9B627AW319

About Nitrendipine

A calcium channel blocker with marked vasodilator action. It is an effective antihypertensive agent and differs from other calcium channel blockers in that it does not reduce glomerular filtration rate and is mildly natriuretic, rather than sodium retentive.

DSSTox_CID_3373 Manufacturers

A DSSTox_CID_3373 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_3373, including repackagers and relabelers. The FDA regulates DSSTox_CID_3373 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_3373 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 DSSTox_CID_3373 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

DSSTox_CID_3373 Suppliers

A DSSTox_CID_3373 supplier is an individual or a company that provides DSSTox_CID_3373 active pharmaceutical ingredient (API) or DSSTox_CID_3373 finished formulations upon request. The DSSTox_CID_3373 suppliers may include DSSTox_CID_3373 API manufacturers, exporters, distributors and traders.

click here to find a list of DSSTox_CID_3373 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

DSSTox_CID_3373 USDMF

A DSSTox_CID_3373 DMF (Drug Master File) is a document detailing the whole manufacturing process of DSSTox_CID_3373 active pharmaceutical ingredient (API) in detail. Different forms of DSSTox_CID_3373 DMFs exist exist since differing nations have different regulations, such as DSSTox_CID_3373 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A DSSTox_CID_3373 DMF submitted to regulatory agencies in the US is known as a USDMF. DSSTox_CID_3373 USDMF includes data on DSSTox_CID_3373's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The DSSTox_CID_3373 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of DSSTox_CID_3373 suppliers with USDMF on PharmaCompass.

DSSTox_CID_3373 JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The DSSTox_CID_3373 Drug Master File in Japan (DSSTox_CID_3373 JDMF) empowers DSSTox_CID_3373 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the DSSTox_CID_3373 JDMF during the approval evaluation for pharmaceutical products. At the time of DSSTox_CID_3373 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of DSSTox_CID_3373 suppliers with JDMF on PharmaCompass.

DSSTox_CID_3373 CEP

A DSSTox_CID_3373 CEP of the European Pharmacopoeia monograph is often referred to as a DSSTox_CID_3373 Certificate of Suitability (COS). The purpose of a DSSTox_CID_3373 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of DSSTox_CID_3373 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of DSSTox_CID_3373 to their clients by showing that a DSSTox_CID_3373 CEP has been issued for it. The manufacturer submits a DSSTox_CID_3373 CEP (COS) as part of the market authorization procedure, and it takes on the role of a DSSTox_CID_3373 CEP holder for the record. Additionally, the data presented in the DSSTox_CID_3373 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the DSSTox_CID_3373 DMF.

A DSSTox_CID_3373 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DSSTox_CID_3373 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 DSSTox_CID_3373 suppliers with CEP (COS) on PharmaCompass.

DSSTox_CID_3373 GMP

DSSTox_CID_3373 Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of DSSTox_CID_3373 GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right DSSTox_CID_3373 GMP manufacturer or DSSTox_CID_3373 GMP API supplier for your needs.

DSSTox_CID_3373 CoA

A DSSTox_CID_3373 CoA (Certificate of Analysis) is a formal document that attests to DSSTox_CID_3373's compliance with DSSTox_CID_3373 specifications and serves as a tool for batch-level quality control.

DSSTox_CID_3373 CoA mostly includes findings from lab analyses of a specific batch. For each DSSTox_CID_3373 CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

DSSTox_CID_3373 may be tested according to a variety of international standards, such as European Pharmacopoeia (DSSTox_CID_3373 EP), DSSTox_CID_3373 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (DSSTox_CID_3373 USP).

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.
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