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Looking for 15676-16-1 / Sulpiride API manufacturers, exporters & distributors?

Sulpiride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Sulpiride

Synonyms

15676-16-1, Sulpyrid, Sulpirid, Aiglonyl, Dolmatil, Dogmatil

Cas Number

15676-16-1

Unique Ingredient Identifier (UNII)

7MNE9M8287

About Sulpiride

A dopamine D2-receptor antagonist. It has been used therapeutically as an antidepressant, antipsychotic, and as a digestive aid. (From Merck Index, 11th ed)

NCGC00024852-05 Manufacturers

A NCGC00024852-05 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NCGC00024852-05, including repackagers and relabelers. The FDA regulates NCGC00024852-05 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NCGC00024852-05 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 NCGC00024852-05 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

NCGC00024852-05 Suppliers

A NCGC00024852-05 supplier is an individual or a company that provides NCGC00024852-05 active pharmaceutical ingredient (API) or NCGC00024852-05 finished formulations upon request. The NCGC00024852-05 suppliers may include NCGC00024852-05 API manufacturers, exporters, distributors and traders.

click here to find a list of NCGC00024852-05 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

NCGC00024852-05 USDMF

A NCGC00024852-05 DMF (Drug Master File) is a document detailing the whole manufacturing process of NCGC00024852-05 active pharmaceutical ingredient (API) in detail. Different forms of NCGC00024852-05 DMFs exist exist since differing nations have different regulations, such as NCGC00024852-05 USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A NCGC00024852-05 DMF submitted to regulatory agencies in the US is known as a USDMF. NCGC00024852-05 USDMF includes data on NCGC00024852-05's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NCGC00024852-05 USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of NCGC00024852-05 suppliers with USDMF on PharmaCompass.

NCGC00024852-05 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 NCGC00024852-05 Drug Master File in Japan (NCGC00024852-05 JDMF) empowers NCGC00024852-05 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 NCGC00024852-05 JDMF during the approval evaluation for pharmaceutical products. At the time of NCGC00024852-05 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 NCGC00024852-05 suppliers with JDMF on PharmaCompass.

NCGC00024852-05 KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a NCGC00024852-05 Drug Master File in Korea (NCGC00024852-05 KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of NCGC00024852-05. The MFDS reviews the NCGC00024852-05 KDMF as part of the drug registration process and uses the information provided in the NCGC00024852-05 KDMF to evaluate the safety and efficacy of the drug.

After submitting a NCGC00024852-05 KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their NCGC00024852-05 API can apply through the Korea Drug Master File (KDMF).

click here to find a list of NCGC00024852-05 suppliers with KDMF on PharmaCompass.

NCGC00024852-05 CEP

A NCGC00024852-05 CEP of the European Pharmacopoeia monograph is often referred to as a NCGC00024852-05 Certificate of Suitability (COS). The purpose of a NCGC00024852-05 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NCGC00024852-05 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NCGC00024852-05 to their clients by showing that a NCGC00024852-05 CEP has been issued for it. The manufacturer submits a NCGC00024852-05 CEP (COS) as part of the market authorization procedure, and it takes on the role of a NCGC00024852-05 CEP holder for the record. Additionally, the data presented in the NCGC00024852-05 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NCGC00024852-05 DMF.

A NCGC00024852-05 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NCGC00024852-05 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 NCGC00024852-05 suppliers with CEP (COS) on PharmaCompass.

NCGC00024852-05 GMP

NCGC00024852-05 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 NCGC00024852-05 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 NCGC00024852-05 GMP manufacturer or NCGC00024852-05 GMP API supplier for your needs.

NCGC00024852-05 CoA

A NCGC00024852-05 CoA (Certificate of Analysis) is a formal document that attests to NCGC00024852-05's compliance with NCGC00024852-05 specifications and serves as a tool for batch-level quality control.

NCGC00024852-05 CoA mostly includes findings from lab analyses of a specific batch. For each NCGC00024852-05 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.

NCGC00024852-05 may be tested according to a variety of international standards, such as European Pharmacopoeia (NCGC00024852-05 EP), NCGC00024852-05 JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NCGC00024852-05 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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