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  • TABLET;ORAL - 0.5MG
  • TABLET;ORAL - 1MG
  • TABLET;ORAL - 2MG
  • INJECTABLE;INJECTION - 2MG/ML
  • INJECTABLE;INJECTION - 4MG/ML

Looking for 846-49-1 / Lorazepam API manufacturers, exporters & distributors?

Lorazepam manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Lorazepam

Synonyms

Ativan, 846-49-1, O-chloroxazepam, O-chlorooxazepam, Temesta, Loraz

Cas Number

846-49-1

Unique Ingredient Identifier (UNII)

O26FZP769L

About Lorazepam

A benzodiazepine used as an anti-anxiety agent with few side effects. It also has hypnotic, anticonvulsant, and considerable sedative properties and has been proposed as a preanesthetic agent.

Alzapam Manufacturers

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

Alzapam Suppliers

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

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

Alzapam USDMF

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

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

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

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

Alzapam CEP

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

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

Alzapam WC

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

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

Alzapam 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 Alzapam as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Alzapam 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 Alzapam 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 Alzapam and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Alzapam NDC to their finished compounded human drug products, they may choose to do so.

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

Alzapam GMP

Alzapam 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 Alzapam 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 Alzapam GMP manufacturer or Alzapam GMP API supplier for your needs.

Alzapam CoA

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

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

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