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Looking for 63323-46-6 / Ciramadol API manufacturers, exporters & distributors?

Ciramadol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Ciramadol

Synonyms

Ciramadol hcl, Ciradol, Ciramadol hydrochloride [usan], 63323-46-6, Wy-15,705 hcl, 090xo8449j

Cas Number

63323-46-6

Unique Ingredient Identifier (UNII)

090XO8449J

090XO8449J Manufacturers

A 090XO8449J manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 090XO8449J, including repackagers and relabelers. The FDA regulates 090XO8449J manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 090XO8449J API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

090XO8449J Suppliers

A 090XO8449J supplier is an individual or a company that provides 090XO8449J active pharmaceutical ingredient (API) or 090XO8449J finished formulations upon request. The 090XO8449J suppliers may include 090XO8449J API manufacturers, exporters, distributors and traders.

click here to find a list of 090XO8449J suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

090XO8449J USDMF

A 090XO8449J DMF (Drug Master File) is a document detailing the whole manufacturing process of 090XO8449J active pharmaceutical ingredient (API) in detail. Different forms of 090XO8449J DMFs exist exist since differing nations have different regulations, such as 090XO8449J USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A 090XO8449J DMF submitted to regulatory agencies in the US is known as a USDMF. 090XO8449J USDMF includes data on 090XO8449J's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 090XO8449J USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of 090XO8449J suppliers with USDMF on PharmaCompass.

090XO8449J GMP

090XO8449J 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 090XO8449J 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 090XO8449J GMP manufacturer or 090XO8449J GMP API supplier for your needs.

090XO8449J CoA

A 090XO8449J CoA (Certificate of Analysis) is a formal document that attests to 090XO8449J's compliance with 090XO8449J specifications and serves as a tool for batch-level quality control.

090XO8449J CoA mostly includes findings from lab analyses of a specific batch. For each 090XO8449J 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.

090XO8449J may be tested according to a variety of international standards, such as European Pharmacopoeia (090XO8449J EP), 090XO8449J JP (Japanese Pharmacopeia) and the US Pharmacopoeia (090XO8449J 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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