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Veranova: A CDMO that manages complexity with confidence.
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Veranova: A CDMO that manages complexity with confidence.
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Veranova: A CDMO that manages complexity with confidence.
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Veranova: A CDMO that manages complexity with confidence.
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Veranova: A CDMO that manages complexity with confidence.
About the Company : Veranova is a global leader in the development and manufacturing of specialist and complex APIs for pharma and biotech customers. We have over 50 years of experience navigating the...
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Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
dl-1-Chloro-1-phenyl-2-aminopropane Hydrochloride
CAS Number : 25394-33-6
End Use API : Amphetamine Sulfate
About The Company : Malladi Drugs & Pharmaceuticals Ltd was founded in 1980 by microbiologist Mr. M L N Sastry. Within a few years, Malladi established itself as a leader in manufa...
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
CAS Number : 3182-95-4
End Use API : Amphetamine Sulfate
About The Company : PMC Isochem is a CDMO company acquired by PMC International in 2017. It manufactures cGMP intermediates, active pharmaceutical ingredients and functional excipi...
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Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
Regulatory Info :
Registration Country : India
Brand Name : Amphetamine
Dosage Form : Tablet
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
Regulatory Info :
Registration Country : India
Brand Name : Amphetamine
Dosage Form : Tablet
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
Regulatory Info :
Registration Country : India
Brand Name : Amphetamine
Dosage Form : Tablet
Dosage Strength : 15MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Mixed Amphetamines
Dosage Form : Extended Release Capsu...
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Mixed Amphetamines
Dosage Form : Extended Release Capsu...
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Mixed Amphetamines
Dosage Form : Extended Release Capsu...
Dosage Strength : 25MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Mixed Amphetamines
Dosage Form : Extended Release Capsu...
Dosage Strength : 30MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Mixed Amphetamines
Dosage Form : Immediate Release Tabl...
Dosage Strength : 5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Mixed Amphetamines
Dosage Form : Immediate Release Tabl...
Dosage Strength : 10MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Mixed Amphetamines
Dosage Form : Immediate Release Tabl...
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
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DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 10M...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 10MG
USFDA APPLICATION NUMBER - 17078
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 15M...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 15MG
USFDA APPLICATION NUMBER - 17078
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 5MG
USFDA APPLICATION NUMBER - 17078
DOSAGE - SUSPENSION, EXTENDED RELEASE;ORAL - ...DOSAGE - SUSPENSION, EXTENDED RELEASE;ORAL - EQ 1.25MG BASE/ML
USFDA APPLICATION NUMBER - 204325
DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTEN...DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL - EQ 12.5MG BASE
USFDA APPLICATION NUMBER - 204326
DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTEN...DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL - EQ 15.7MG BASE
USFDA APPLICATION NUMBER - 204326
DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTEN...DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL - EQ 18.8MG BASE
USFDA APPLICATION NUMBER - 204326
DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTEN...DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL - EQ 3.1MG BASE
USFDA APPLICATION NUMBER - 204326
DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTEN...DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL - EQ 6.3MG BASE
USFDA APPLICATION NUMBER - 204326
DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTEN...DOSAGE - TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL - EQ 9.4MG BASE
USFDA APPLICATION NUMBER - 204326
DOSAGE - SUSPENSION, EXTENDED RELEASE;ORAL - ...DOSAGE - SUSPENSION, EXTENDED RELEASE;ORAL - 2MG/ML;EQ 0.5MG BASE/ML
USFDA APPLICATION NUMBER - 208147
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 12MG...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 12MG;EQ 3MG BASE
USFDA APPLICATION NUMBER - 210526
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 16MG...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 16MG;EQ 4MG BASE
USFDA APPLICATION NUMBER - 210526
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 4MG;...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 4MG;EQ 1MG BASE
USFDA APPLICATION NUMBER - 210526
DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 8MG;...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 8MG;EQ 2MG BASE
USFDA APPLICATION NUMBER - 210526
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 1.2...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 1.25MG;1.25MG;1.25MG;1.25MG
USFDA APPLICATION NUMBER - 21303
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 2.5...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 2.5MG;2.5MG;2.5MG;2.5MG
USFDA APPLICATION NUMBER - 21303
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 3.7...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 3.75MG;3.75MG;3.75MG;3.75MG
USFDA APPLICATION NUMBER - 21303
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 5MG...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 5MG;5MG;5MG;5MG
USFDA APPLICATION NUMBER - 21303
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 6.2...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 6.25MG;6.25MG;6.25MG;6.25MG
USFDA APPLICATION NUMBER - 21303
DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 7.5...DOSAGE - CAPSULE, EXTENDED RELEASE;ORAL - 7.5MG;7.5MG;7.5MG;7.5MG
USFDA APPLICATION NUMBER - 21303
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Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
Amphetamine, Dextroamphetamine Saccharate, Amphetamine Aspartate Monohydrate, Dextroamphetamine Sulfate, Amphetamine Sulfate
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REF. STANDARDS & IMPURITIES
Others
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
CAS Number : 22148-75-0
Quantity Per Vial :
Sale Unit :
Price :
Details : N-formylamphetamine
Monograph : 51634-2040
Storage :
Code/Batch No :
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
CAS Number : 60-13-9
Quantity Per Vial :
Sale Unit :
Price :
Details : USP Impurity
Monograph : 51634-2024
Storage :
Code/Batch No :
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
Dextroamphetamine Sulfate (CII)
CAS Number : 51-63-8
Quantity Per Vial :
Sale Unit :
Price :
Details : USP Impurity
Monograph : 51634-2022
Storage :
Code/Batch No :
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
Dextroamphetamine Sulfate, < 98% EE (CII)
CAS Number : 51-63-8
Quantity Per Vial :
Sale Unit :
Price :
Details :
Monograph : 51634-2022
Storage :
Code/Batch No :
FULL SCREEN VIEW Click here to open all results in a new tab [this preview display 10 results]ABOUT THIS PAGE
54
PharmaCompass offers a list of Amphetamine Sulfate 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 Amphetamine Sulfate manufacturer or Amphetamine Sulfate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amphetamine Sulfate manufacturer or Amphetamine Sulfate supplier.
PharmaCompass also assists you with knowing the Amphetamine Sulfate API Price utilized in the formulation of products. Amphetamine Sulfate API Price is not always fixed or binding as the Amphetamine Sulfate Price is obtained through a variety of data sources. The Amphetamine Sulfate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A dl-alpha-Methylphenethylamine sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of dl-alpha-Methylphenethylamine sulfate, including repackagers and relabelers. The FDA regulates dl-alpha-Methylphenethylamine sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. dl-alpha-Methylphenethylamine sulfate 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 dl-alpha-Methylphenethylamine sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A dl-alpha-Methylphenethylamine sulfate supplier is an individual or a company that provides dl-alpha-Methylphenethylamine sulfate active pharmaceutical ingredient (API) or dl-alpha-Methylphenethylamine sulfate finished formulations upon request. The dl-alpha-Methylphenethylamine sulfate suppliers may include dl-alpha-Methylphenethylamine sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of dl-alpha-Methylphenethylamine sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A dl-alpha-Methylphenethylamine sulfate DMF (Drug Master File) is a document detailing the whole manufacturing process of dl-alpha-Methylphenethylamine sulfate active pharmaceutical ingredient (API) in detail. Different forms of dl-alpha-Methylphenethylamine sulfate DMFs exist exist since differing nations have different regulations, such as dl-alpha-Methylphenethylamine sulfate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A dl-alpha-Methylphenethylamine sulfate DMF submitted to regulatory agencies in the US is known as a USDMF. dl-alpha-Methylphenethylamine sulfate USDMF includes data on dl-alpha-Methylphenethylamine sulfate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The dl-alpha-Methylphenethylamine sulfate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of dl-alpha-Methylphenethylamine sulfate suppliers with USDMF on PharmaCompass.
A dl-alpha-Methylphenethylamine sulfate CEP of the European Pharmacopoeia monograph is often referred to as a dl-alpha-Methylphenethylamine sulfate Certificate of Suitability (COS). The purpose of a dl-alpha-Methylphenethylamine sulfate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of dl-alpha-Methylphenethylamine sulfate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of dl-alpha-Methylphenethylamine sulfate to their clients by showing that a dl-alpha-Methylphenethylamine sulfate CEP has been issued for it. The manufacturer submits a dl-alpha-Methylphenethylamine sulfate CEP (COS) as part of the market authorization procedure, and it takes on the role of a dl-alpha-Methylphenethylamine sulfate CEP holder for the record. Additionally, the data presented in the dl-alpha-Methylphenethylamine sulfate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the dl-alpha-Methylphenethylamine sulfate DMF.
A dl-alpha-Methylphenethylamine sulfate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. dl-alpha-Methylphenethylamine sulfate 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 dl-alpha-Methylphenethylamine sulfate suppliers with CEP (COS) 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 dl-alpha-Methylphenethylamine sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for dl-alpha-Methylphenethylamine sulfate 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 dl-alpha-Methylphenethylamine sulfate 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 dl-alpha-Methylphenethylamine sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a dl-alpha-Methylphenethylamine sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of dl-alpha-Methylphenethylamine sulfate suppliers with NDC on PharmaCompass.
dl-alpha-Methylphenethylamine sulfate 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 dl-alpha-Methylphenethylamine sulfate 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 dl-alpha-Methylphenethylamine sulfate GMP manufacturer or dl-alpha-Methylphenethylamine sulfate GMP API supplier for your needs.
A dl-alpha-Methylphenethylamine sulfate CoA (Certificate of Analysis) is a formal document that attests to dl-alpha-Methylphenethylamine sulfate's compliance with dl-alpha-Methylphenethylamine sulfate specifications and serves as a tool for batch-level quality control.
dl-alpha-Methylphenethylamine sulfate CoA mostly includes findings from lab analyses of a specific batch. For each dl-alpha-Methylphenethylamine sulfate 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.
dl-alpha-Methylphenethylamine sulfate may be tested according to a variety of international standards, such as European Pharmacopoeia (dl-alpha-Methylphenethylamine sulfate EP), dl-alpha-Methylphenethylamine sulfate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (dl-alpha-Methylphenethylamine sulfate USP).
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