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Looking for 127676-30-6 / Pioglitazone Hydrochloride API manufacturers, exporters & distributors?

Pioglitazone Hydrochloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Pioglitazone Hydrochloride

Synonyms

112529-15-4, Pioglitazone hcl, Actos, Piomed, 5-(4-(2-(5-ethylpyridin-2-yl)ethoxy)benzyl)thiazolidine-2,4-dione hydrochloride, U-72107a

Cas Number

127676-30-6

Unique Ingredient Identifier (UNII)

JQT35NPK6C

About Pioglitazone Hydrochloride

A thiazolidinedione and PPAR GAMMA agonist that is used in the treatment of TYPE 2 DIABETES MELLITUS.

Pioglitazone Hydrochloride Manufacturers

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

Pioglitazone Hydrochloride Suppliers

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

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

Pioglitazone Hydrochloride USDMF

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

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

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

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

Pioglitazone Hydrochloride KDMF

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

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

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

click here to find a list of Pioglitazone Hydrochloride suppliers with KDMF on PharmaCompass.

Pioglitazone Hydrochloride CEP

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

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

Pioglitazone Hydrochloride WC

A Pioglitazone Hydrochloride written confirmation (Pioglitazone Hydrochloride WC) is an official document issued by a regulatory agency to a Pioglitazone Hydrochloride manufacturer, verifying that the manufacturing facility of a Pioglitazone Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Pioglitazone Hydrochloride APIs or Pioglitazone Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Pioglitazone Hydrochloride WC (written confirmation) as part of the regulatory process.

click here to find a list of Pioglitazone Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.

Pioglitazone Hydrochloride NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Pioglitazone Hydrochloride as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Pioglitazone Hydrochloride API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Pioglitazone Hydrochloride as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Pioglitazone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pioglitazone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Pioglitazone Hydrochloride suppliers with NDC on PharmaCompass.

Pioglitazone Hydrochloride GMP

Pioglitazone Hydrochloride 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 Pioglitazone Hydrochloride 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 Pioglitazone Hydrochloride GMP manufacturer or Pioglitazone Hydrochloride GMP API supplier for your needs.

Pioglitazone Hydrochloride CoA

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

Pioglitazone Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Pioglitazone Hydrochloride 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.

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