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    Chemistry

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    Also known as: Schembl34274, Ft-0603494, Ft-0656045
    Molecular Formula
    C34H48N2O10S
    Molecular Weight
    676.8  g/mol
    InChI Key
    HOBWAPHTEJGALG-UHFFFAOYSA-N
    Atropine Sulfate
    1 2D Structure

    Atropine Sulfate

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    (8-methyl-8-azoniabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate;sulfate
    2.1.2 InChI
    InChI=1S/2C17H23NO3.H2O4S/c2*1-18-13-7-8-14(18)10-15(9-13)21-17(20)16(11-19)12-5-3-2-4-6-12;1-5(2,3)4/h2*2-6,13-16,19H,7-11H2,1H3;(H2,1,2,3,4)
    2.1.3 InChI Key
    HOBWAPHTEJGALG-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    C[NH+]1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3.C[NH+]1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3.[O-]S(=O)(=O)[O-]
    2.2 Synonyms
    2.2.1 Depositor-Supplied Synonyms

    1. Schembl34274

    2. Ft-0603494

    3. Ft-0656045

    2.3 Create Date
    2012-08-08
    3 Chemical and Physical Properties
    Molecular Weight 676.8 g/mol
    Molecular Formula C34H48N2O10S
    Hydrogen Bond Donor Count4
    Hydrogen Bond Acceptor Count10
    Rotatable Bond Count10
    Exact Mass676.30296691 g/mol
    Monoisotopic Mass676.30296691 g/mol
    Topological Polar Surface Area191 Ų
    Heavy Atom Count47
    Formal Charge0
    Complexity415
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count6
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count3
    4 Drug and Medication Information
    4.1 Drug Information
    1 of 2  
    Drug NameAtropine sulfate
    Drug LabelAtropine Sulfate Injection, USP is a sterile, nonpyrogenic isotonic solution of atropine sulfate monohydrate in water for injection with sodium chloride sufficient to render the solution isotonic. It is administered parenterally by subcutaneous, intr...
    Active IngredientAtropine sulfate
    Dosage FormSolution/drops
    RouteOphthalmic
    Strength1%
    Market StatusPrescription
    CompanyAkorn

    2 of 2  
    Drug NameAtropine sulfate
    Drug LabelAtropine Sulfate Injection, USP is a sterile, nonpyrogenic isotonic solution of atropine sulfate monohydrate in water for injection with sodium chloride sufficient to render the solution isotonic. It is administered parenterally by subcutaneous, intr...
    Active IngredientAtropine sulfate
    Dosage FormSolution/drops
    RouteOphthalmic
    Strength1%
    Market StatusPrescription
    CompanyAkorn

    API Reference Price

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Import","activeIngredients":"","year":"2024","qtr":"Q4","strtotime":1732041000,"product":"(SAMPLE FOR R & D DOVELOPMENT ONLY) ATROPINE SULFATE(BATCH NO.A008640523\/30GM(AS PER INVOICE)","address":"PLOT NO 117 S.NO 53 13 NIZAMPET,","city":"HYDERABAD,TELANGANA","supplier":"C SQUARED PHARMA LTD","supplierCountry":"INDIA","foreign_port":"FRANKFURT\/MAIN INT\\'L","customer":"PROPHARMEX INDIA PRIVATE LTD","customerCountry":"INDIA","quantity":"0.03","actualQuantity":"30","unit":"GMS","unitRateFc":"20","totalValueFC":"699.4","currency":"EURO","unitRateINR":"1967.3","date":"20-Nov-2024","totalValueINR":"59020","totalValueInUsd":"699.4","indian_port":"Hyderabad Air","hs_no":"29397900","bill_no":"6767534","productDescription":"Re-Import","marketType":"REGULATED MARKET","country":"INDIA","selfForZScoreResived":"Pharma Grade","supplierPort":"FRANKFURT\/MAIN INT\\'L","supplierAddress":"BRIDGE HOUSE UNIT-2 SKEHARD ROAD T12 H2TK CORK, IRELAND IE","customerAddress":"PLOT NO 117 S.NO 53 13 NIZAMPET,"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q4","strtotime":1734460200,"product":"ATROPINE SULFATE (0.700 KGS ) ( FOR R & D PURPOSE TEST LIC.SW\/OD\/11\/2024\/000003869 )ATROPINE SULFATE (0.700 KGS ) ( FOR R & D PURPOSE TEST LIC.S","address":"142-48 S.V.ROAD,","city":"MUMBAI, MAHARASHTRA","supplier":"ROLABO OUTSOURCING SL","supplierCountry":"SPAIN","foreign_port":"BARCELONA","customer":"FDC LTD","customerCountry":"INDIA","quantity":"0.70","actualQuantity":"0.7","unit":"KGS","unitRateFc":"13789.3","totalValueFC":"9729.8","currency":"USD","unitRateINR":"1181050","date":"18-Dec-2024","totalValueINR":"826735","totalValueInUsd":"9729.8","indian_port":"Bombay Air","hs_no":"29397900","bill_no":"7311345","productDescription":"API","marketType":"REGULATED MARKET","country":"SPAIN","selfForZScoreResived":"Pharma Grade","supplierPort":"BARCELONA","supplierAddress":"POL IND MALPICA, CALLE J,3-4 ZARAGO ZA SDNF SPAIN","customerAddress":"142-48 S.V.ROAD,"},{"dataSource":"API Import","activeIngredients":"","year":"2025","qtr":"Q1","strtotime":1739817000,"product":"31016 ATROPINE SULFATE API (IMP LIC.NO.SW\/OD\/11\/2024\/000006614)31016 ATROPINE SULFATE (IMP LIC.NO.SW\/OD\/11\/2024\/000006614)","address":"208, OKHLA INDUSTRIAL ESTATE,,PHAS","city":"NEW DELHI,DELHI","supplier":"ROLABO OUTSOURCING SL","supplierCountry":"SPAIN","foreign_port":"BARCELONA","customer":"MANKIND PHARMA LTD","customerCountry":"INDIA","quantity":"3.32","actualQuantity":"3.32","unit":"KGS","unitRateFc":"11760","totalValueFC":"39687.9","currency":"USD","unitRateINR":"1039584","date":"18-Feb-2025","totalValueINR":"3451418.88","totalValueInUsd":"39687.9","indian_port":"Delhi Air","hs_no":"29397900","bill_no":"8423352","productDescription":"API","marketType":"REGULATED MARKET","country":"SPAIN","selfForZScoreResived":"Pharma Grade","supplierPort":"BARCELONA","supplierAddress":"POL. IND. MALPICA, CALLE J 3-4 - 50016 ZARAGOZA ESPANA SPAIN","customerAddress":"208, OKHLA INDUSTRIAL ESTATE,,PHAS"}]
    12-Jan-2022
    19-May-2025
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    DOSAGE - TABLET;ORAL - 0.025MG;2.5MG

    USFDA APPLICATION NUMBER - 12462

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    DOSAGE - INJECTABLE;INJECTION - 0.14MG/ML;10M...DOSAGE - INJECTABLE;INJECTION - 0.14MG/ML;10MG/ML

    USFDA APPLICATION NUMBER - 19678

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    DOSAGE - SOLUTION;INTRAVENOUS - 0.25MG/5ML (0...DOSAGE - SOLUTION;INTRAVENOUS - 0.25MG/5ML (0.05MG/ML)

    USFDA APPLICATION NUMBER - 21146

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    DOSAGE - SOLUTION;INTRAVENOUS - 0.5MG/5ML (0....DOSAGE - SOLUTION;INTRAVENOUS - 0.5MG/5ML (0.1MG/ML)

    USFDA APPLICATION NUMBER - 21146

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    DOSAGE - SOLUTION;INTRAVENOUS - 1MG/10ML (0.1...DOSAGE - SOLUTION;INTRAVENOUS - 1MG/10ML (0.1MG/ML)

    USFDA APPLICATION NUMBER - 21146

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    ABOUT THIS PAGE

    Looking for / Atropine Sulfate API manufacturers, exporters & distributors?

    Atropine Sulfate manufacturers, exporters & distributors 1

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

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

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

    API | Excipient name

    Atropine Sulfate

    Synonyms

    Schembl34274, Ft-0603494, Ft-0656045

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE Manufacturers

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

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE Suppliers

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

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

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE USDMF

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

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

    click here to find a list of DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE suppliers with USDMF on PharmaCompass.

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

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE KDMF

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

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

    After submitting a DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE 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 DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE API can apply through the Korea Drug Master File (KDMF).

    click here to find a list of DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE suppliers with KDMF on PharmaCompass.

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE CEP

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

    A DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. DIPHENOXYLATE HYDROCHLORIDE; ATROPINE 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 DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE suppliers with CEP (COS) on PharmaCompass.

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE WC

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

    click here to find a list of DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE suppliers with Written Confirmation (WC) on PharmaCompass.

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE 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 DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE as an active pharmaceutical ingredient (API).

    Finished drug products

    The FDA updates the NDC directory daily. The NDC numbers for DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE 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 DIPHENOXYLATE HYDROCHLORIDE; ATROPINE 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.

    Compounded drug products

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

    click here to find a list of DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE suppliers with NDC on PharmaCompass.

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE GMP

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE 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 DIPHENOXYLATE HYDROCHLORIDE; ATROPINE 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 DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE GMP manufacturer or DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE GMP API supplier for your needs.

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE CoA

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

    DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE CoA mostly includes findings from lab analyses of a specific batch. For each DIPHENOXYLATE HYDROCHLORIDE; ATROPINE 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.

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