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API SUPPLIERS
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USDMF
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Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methylprednisolone Acetate BP/EP/USP
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A
Address of the Firm : 385/2, Gram Pigdamber, Rau , Indore-453331, Madhya Pradesh, India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methyl Prednisolone Acetate USP
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm : 385/2, Gram Pigdamber, Rau, Indore-453331, M.P., India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methylprednisolone Acetate BP/EP/USP
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161n
Address of the Firm : PLOT NO.385/2, Gram Pigdamber, Rau , Indore-453331, Madhya Pradesh, India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methyl Prednisolone Acetate USP
Date of Issue : 2022-07-23
Valid Till : 2025-02-07
Written Confirmation Number : WC-0162n
Address of the Firm : Plot No-5,6,7 & 8, Special Economic Zone, Phase-II, Pharma Zone, Pithampur, Dist...
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
Methylprednisolone Acetate USP
Date of Issue : 2022-08-31
Valid Till : 2025-02-07
Written Confirmation Number : WC-0162A2
Address of the Firm : Plot No. 5,6,7 &8, Special Economic Zone, Phase II, Pharma Zone, Pithampur, Dist...
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API/FDF Prices: Book a Demo to explore the features and consider upgrading later
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DOSAGE - INJECTABLE;INJECTION - 20MG/ML
USFDA APPLICATION NUMBER - 11757
DOSAGE - INJECTABLE;INJECTION - 40MG/ML
USFDA APPLICATION NUMBER - 11757
DOSAGE - INJECTABLE;INJECTION - 80MG/ML
USFDA APPLICATION NUMBER - 11757
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PharmaCompass offers a list of Methylprednisolone Acetate 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 Methylprednisolone Acetate manufacturer or Methylprednisolone Acetate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methylprednisolone Acetate manufacturer or Methylprednisolone Acetate supplier.
PharmaCompass also assists you with knowing the Methylprednisolone Acetate API Price utilized in the formulation of products. Methylprednisolone Acetate API Price is not always fixed or binding as the Methylprednisolone Acetate Price is obtained through a variety of data sources. The Methylprednisolone Acetate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A NEO-MEDROL ACETATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of NEO-MEDROL ACETATE, including repackagers and relabelers. The FDA regulates NEO-MEDROL ACETATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. NEO-MEDROL ACETATE 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 NEO-MEDROL ACETATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A NEO-MEDROL ACETATE supplier is an individual or a company that provides NEO-MEDROL ACETATE active pharmaceutical ingredient (API) or NEO-MEDROL ACETATE finished formulations upon request. The NEO-MEDROL ACETATE suppliers may include NEO-MEDROL ACETATE API manufacturers, exporters, distributors and traders.
click here to find a list of NEO-MEDROL ACETATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A NEO-MEDROL ACETATE DMF (Drug Master File) is a document detailing the whole manufacturing process of NEO-MEDROL ACETATE active pharmaceutical ingredient (API) in detail. Different forms of NEO-MEDROL ACETATE DMFs exist exist since differing nations have different regulations, such as NEO-MEDROL ACETATE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A NEO-MEDROL ACETATE DMF submitted to regulatory agencies in the US is known as a USDMF. NEO-MEDROL ACETATE USDMF includes data on NEO-MEDROL ACETATE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The NEO-MEDROL ACETATE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of NEO-MEDROL ACETATE suppliers with USDMF on PharmaCompass.
A NEO-MEDROL ACETATE CEP of the European Pharmacopoeia monograph is often referred to as a NEO-MEDROL ACETATE Certificate of Suitability (COS). The purpose of a NEO-MEDROL ACETATE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of NEO-MEDROL ACETATE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of NEO-MEDROL ACETATE to their clients by showing that a NEO-MEDROL ACETATE CEP has been issued for it. The manufacturer submits a NEO-MEDROL ACETATE CEP (COS) as part of the market authorization procedure, and it takes on the role of a NEO-MEDROL ACETATE CEP holder for the record. Additionally, the data presented in the NEO-MEDROL ACETATE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the NEO-MEDROL ACETATE DMF.
A NEO-MEDROL ACETATE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. NEO-MEDROL ACETATE 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 NEO-MEDROL ACETATE suppliers with CEP (COS) on PharmaCompass.
A NEO-MEDROL ACETATE written confirmation (NEO-MEDROL ACETATE WC) is an official document issued by a regulatory agency to a NEO-MEDROL ACETATE manufacturer, verifying that the manufacturing facility of a NEO-MEDROL ACETATE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting NEO-MEDROL ACETATE APIs or NEO-MEDROL ACETATE finished pharmaceutical products to another nation, regulatory agencies frequently require a NEO-MEDROL ACETATE WC (written confirmation) as part of the regulatory process.
click here to find a list of NEO-MEDROL ACETATE suppliers with Written Confirmation (WC) on PharmaCompass.
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 NEO-MEDROL ACETATE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for NEO-MEDROL ACETATE API and other APIs are published in this directory by the FDA.
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 NEO-MEDROL ACETATE 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.
The NDC directory also contains data on finished compounded human drug products that contain NEO-MEDROL ACETATE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a NEO-MEDROL ACETATE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of NEO-MEDROL ACETATE suppliers with NDC on PharmaCompass.
NEO-MEDROL ACETATE 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 NEO-MEDROL ACETATE 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 NEO-MEDROL ACETATE GMP manufacturer or NEO-MEDROL ACETATE GMP API supplier for your needs.
A NEO-MEDROL ACETATE CoA (Certificate of Analysis) is a formal document that attests to NEO-MEDROL ACETATE's compliance with NEO-MEDROL ACETATE specifications and serves as a tool for batch-level quality control.
NEO-MEDROL ACETATE CoA mostly includes findings from lab analyses of a specific batch. For each NEO-MEDROL ACETATE 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.
NEO-MEDROL ACETATE may be tested according to a variety of international standards, such as European Pharmacopoeia (NEO-MEDROL ACETATE EP), NEO-MEDROL ACETATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (NEO-MEDROL ACETATE USP).
