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Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients, & custom-made solutions to our customers.
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Pfanstiehl, a global leader in the manufacture of cGMP high purity, low endotoxin, low metals (HPLE-LM)TM injectable grade excipients.
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DOSAGE - LOTION;TOPICAL - EQ 12% BASE **Feder...DOSAGE - LOTION;TOPICAL - EQ 12% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 19155
DOSAGE - CREAM;TOPICAL - EQ 12% BASE **Federa...DOSAGE - CREAM;TOPICAL - EQ 12% BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
USFDA APPLICATION NUMBER - 20508
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EUROAPI
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ABOUT THIS PAGE
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PharmaCompass offers a list of Ammonium Lactate 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 Ammonium Lactate manufacturer or Ammonium Lactate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ammonium Lactate manufacturer or Ammonium Lactate supplier.
PharmaCompass also assists you with knowing the Ammonium Lactate API Price utilized in the formulation of products. Ammonium Lactate API Price is not always fixed or binding as the Ammonium Lactate Price is obtained through a variety of data sources. The Ammonium Lactate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Lac-hydrin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lac-hydrin, including repackagers and relabelers. The FDA regulates Lac-hydrin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lac-hydrin 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 Lac-hydrin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lac-hydrin supplier is an individual or a company that provides Lac-hydrin active pharmaceutical ingredient (API) or Lac-hydrin finished formulations upon request. The Lac-hydrin suppliers may include Lac-hydrin API manufacturers, exporters, distributors and traders.
click here to find a list of Lac-hydrin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lac-hydrin DMF (Drug Master File) is a document detailing the whole manufacturing process of Lac-hydrin active pharmaceutical ingredient (API) in detail. Different forms of Lac-hydrin DMFs exist exist since differing nations have different regulations, such as Lac-hydrin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lac-hydrin DMF submitted to regulatory agencies in the US is known as a USDMF. Lac-hydrin USDMF includes data on Lac-hydrin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lac-hydrin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lac-hydrin suppliers with USDMF on PharmaCompass.
Lac-hydrin 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 Lac-hydrin 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 Lac-hydrin GMP manufacturer or Lac-hydrin GMP API supplier for your needs.
A Lac-hydrin CoA (Certificate of Analysis) is a formal document that attests to Lac-hydrin's compliance with Lac-hydrin specifications and serves as a tool for batch-level quality control.
Lac-hydrin CoA mostly includes findings from lab analyses of a specific batch. For each Lac-hydrin 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.
Lac-hydrin may be tested according to a variety of international standards, such as European Pharmacopoeia (Lac-hydrin EP), Lac-hydrin JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Lac-hydrin USP).
