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Looking for 60676-86-0 / Silicon Dioxide API API manufacturers, exporters & distributors?

Silicon Dioxide API manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Silicon Dioxide API 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 Silicon Dioxide API manufacturer or Silicon Dioxide API supplier for your needs.

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

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

API | Excipient name

Silicon Dioxide API

Synonyms

Silica, Quartz, Dioxosilane, 7631-86-9, Diatomaceous earth, Silica gel

Cas Number

60676-86-0

Unique Ingredient Identifier (UNII)

ETJ7Z6XBU4

About Silicon Dioxide API

Silicon Dioxide is a natural compound of silicon and oxygen found mostly in sand, Silica has three main crystalline varieties: quartz, tridymite, and cristobalite. Fine particulate silica dust from quartz rock causes over a long-term progressive lung injury, silicosis. (NCI04)

03561_FLUKA Manufacturers

A 03561_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 03561_FLUKA, including repackagers and relabelers. The FDA regulates 03561_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 03561_FLUKA 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 03561_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

03561_FLUKA Suppliers

A 03561_FLUKA supplier is an individual or a company that provides 03561_FLUKA active pharmaceutical ingredient (API) or 03561_FLUKA finished formulations upon request. The 03561_FLUKA suppliers may include 03561_FLUKA API manufacturers, exporters, distributors and traders.

click here to find a list of 03561_FLUKA suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

03561_FLUKA USDMF

A 03561_FLUKA DMF (Drug Master File) is a document detailing the whole manufacturing process of 03561_FLUKA active pharmaceutical ingredient (API) in detail. Different forms of 03561_FLUKA DMFs exist exist since differing nations have different regulations, such as 03561_FLUKA USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 03561_FLUKA DMF submitted to regulatory agencies in the US is known as a USDMF. 03561_FLUKA USDMF includes data on 03561_FLUKA's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 03561_FLUKA USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 03561_FLUKA suppliers with USDMF on PharmaCompass.

03561_FLUKA KDMF

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

Pharmaceutical companies submit a 03561_FLUKA Drug Master File in Korea (03561_FLUKA KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of 03561_FLUKA. The MFDS reviews the 03561_FLUKA KDMF as part of the drug registration process and uses the information provided in the 03561_FLUKA KDMF to evaluate the safety and efficacy of the drug.

After submitting a 03561_FLUKA 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 03561_FLUKA API can apply through the Korea Drug Master File (KDMF).

click here to find a list of 03561_FLUKA suppliers with KDMF on PharmaCompass.

03561_FLUKA CEP

A 03561_FLUKA CEP of the European Pharmacopoeia monograph is often referred to as a 03561_FLUKA Certificate of Suitability (COS). The purpose of a 03561_FLUKA CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 03561_FLUKA EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 03561_FLUKA to their clients by showing that a 03561_FLUKA CEP has been issued for it. The manufacturer submits a 03561_FLUKA CEP (COS) as part of the market authorization procedure, and it takes on the role of a 03561_FLUKA CEP holder for the record. Additionally, the data presented in the 03561_FLUKA CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 03561_FLUKA DMF.

A 03561_FLUKA CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 03561_FLUKA 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 03561_FLUKA suppliers with CEP (COS) on PharmaCompass.

03561_FLUKA GMP

03561_FLUKA 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 03561_FLUKA 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 03561_FLUKA GMP manufacturer or 03561_FLUKA GMP API supplier for your needs.

03561_FLUKA CoA

A 03561_FLUKA CoA (Certificate of Analysis) is a formal document that attests to 03561_FLUKA's compliance with 03561_FLUKA specifications and serves as a tool for batch-level quality control.

03561_FLUKA CoA mostly includes findings from lab analyses of a specific batch. For each 03561_FLUKA 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.

03561_FLUKA may be tested according to a variety of international standards, such as European Pharmacopoeia (03561_FLUKA EP), 03561_FLUKA JP (Japanese Pharmacopeia) and the US Pharmacopoeia (03561_FLUKA 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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