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    Chemistry

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    Also known as: 76-22-2, 2-camphanone, Dl-camphor, (+/-)-camphor, 2-bornanone, 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
    Molecular Formula
    C10H16O
    Molecular Weight
    152.23  g/mol
    InChI Key
    DSSYKIVIOFKYAU-UHFFFAOYSA-N
    Camphor
    A bicyclic monoterpene ketone found widely in plants, especially CINNAMOMUM CAMPHORA. It is used topically as a skin antipruritic and as an anti-infective agent.
    1 2D Structure

    Camphor

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    1,7,7-trimethylbicyclo[2.2.1]heptan-2-one
    2.1.2 InChI
    InChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3
    2.1.3 InChI Key
    DSSYKIVIOFKYAU-UHFFFAOYSA-N
    2.1.4 Canonical SMILES
    CC1(C2CCC1(C(=O)C2)C)C
    2.2 Synonyms
    2.2.1 MeSH Synonyms

    1. Camphor, (+-)-isomer

    2. Camphor, (1r)-isomer

    3. Camphor, (1s)-isomer

    2.2.2 Depositor-Supplied Synonyms

    1. 76-22-2

    2. 2-camphanone

    3. Dl-camphor

    4. (+/-)-camphor

    5. 2-bornanone

    6. 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

    7. (+)-camphor

    8. Bornan-2-one

    9. Root Bark Oil

    10. Kampfer

    11. 21368-68-3

    12. Spirit Of Camphor

    13. 2-camphonone

    14. Gum Camphor

    15. 464-48-2

    16. L-(-)-camphor

    17. 1,7,7-trimethylnorcamphor

    18. Alphanon

    19. 1,7,7-trimethylbicyclo[2.2.1]-2-heptanone

    20. D-(+)-camphor

    21. 2-keto-1,7,7-trimethylnorcamphane

    22. Formosa Camphor

    23. Laurel Camphor

    24. Matricaria Camphor

    25. Camphor, Synthetic

    26. 4,7,7-trimethylbicyclo[2.2.1]heptan-3-one

    27. Bornane, 2-oxo-

    28. Camphor (synthetic)

    29. Huile De Camphre

    30. Chebi:36773

    31. 2-kamfanon

    32. Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-

    33. Dl-bornan-2-one

    34. (-)-alcanfor

    35. Norcamphor, 1,7,7-trimethyl-

    36. Camphor, (1r,4r)-(+)-

    37. Synthetic Camphor

    38. 1,7,7-trimethylbicyclo(2.2.1)heptan-2-one

    39. Camphor Oil

    40. Camphor Powder

    41. Formosa

    42. Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (.+/-.)-

    43. Japan Camphor

    44. Camphor (usp)

    45. Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1r)-

    46. Racemic Camphor

    47. Disperseyellow3

    48. Dl-2-bornanone

    49. Heet (salt/mix)

    50. Dextro,laevo-camphor

    51. Sarna (salt/mix)

    52. (?)-camphor

    53. Dl-camphor (jp17)

    54. (.+/-.)-camphor

    55. Camphor Powder - Synthetic

    56. (1rs,4rs)-1,7,7-trimethylbicyclo(2.2.1)heptan-2-one

    57. Dsstox_cid_10955

    58. Dsstox_rid_78860

    59. Dsstox_gsid_30955

    60. Schembl16068

    61. Camphor, (.+/-.)-

    62. Mls001055495

    63. Chembl15768

    64. Divk1c_000724

    65. Gtpl2422

    66. Dtxsid5030955

    67. Hms502e06

    68. Kbio1_000724

    69. Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1s)-

    70. Ninds_000724

    71. Hms2268a06

    72. Hms3885j06

    73. Hy-n0808

    74. Tox21_200237

    75. Bbl012963

    76. Mfcd00074738

    77. S3851

    78. S4516

    79. Stk803534

    80. ( Inverted Exclamation Marka)-camphor

    81. Akos000118728

    82. Akos022060577

    83. Ac-5284

    84. Ccg-266237

    85. Ccg-266238

    86. Db14156

    87. Lmpr0102120001

    88. Un 2717

    89. Cas-76-22-2

    90. Idi1_000724

    91. Ncgc00090681-05

    92. Ncgc00090730-01

    93. Ncgc00090730-02

    94. Ncgc00090730-05

    95. Ncgc00257791-01

    96. Ac-15523

    97. Smr000386909

    98. Vs-03622

    99. (1r,4r)-1,7,7-trimethylnorbornan-2-one

    100. Db-051377

    101. Db-056037

    102. Db-070734

    103. C1251

    104. Cs-0009813

    105. Ft-0607017

    106. Ft-0607018

    107. Ft-0608303

    108. 4,7,7-trimethyl-3-bicyclo[2.2.1]heptanone

    109. 1,7,7-trimethyl-bicyclo[2.2.1]heptan-6-one

    110. C00809

    111. C18369

    112. D00098

    113. E75814

    114. 1,7,7-trimethyl-bicyclo[2.2.1]heptan-2-one

    115. A838646

    116. Q181559

    117. Q-200784

    118. W-109539

    119. W-110530

    120. (+/-)-1,7,7-trimethyl-bicyclo[2,2,1]heptane-2-one

    121. F0001-0763

    122. Z940713494

    2.3 Create Date
    2005-03-25
    3 Chemical and Physical Properties
    Molecular Weight 152.23 g/mol
    Molecular Formula C10H16O
    XLogP32.2
    Hydrogen Bond Donor Count0
    Hydrogen Bond Acceptor Count1
    Rotatable Bond Count0
    Exact Mass152.120115130 g/mol
    Monoisotopic Mass152.120115130 g/mol
    Topological Polar Surface Area17.1 Ų
    Heavy Atom Count11
    Formal Charge0
    Complexity217
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count2
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Drug and Medication Information
    4.1 Therapeutic Uses

    Anti-Infective Agents, Local

    National Library of Medicine's Medical Subject Headings online file (MeSH, 2014); Available from, as of July 31, 2014: https://www.nlm.nih.gov/cgi/mesh/2014/MB_cgi?term=Camphor

    It /SRP: was formerly/ used ... In humans for inflamed joints, sprains, and rheumatic and other inflammatory conditions such as colds in throat and chest. ... patient may feel improved /however/ inflammation is not affected.

    Osol, A. (ed.). Remington's Pharmaceutical Sciences. 16th ed. Easton, Pennsylvania: Mack Publishing Co., 1980., p. 724

    MEDICATION (VET): Locally, camphor is weakly antiseptic and has a rubefacient action when applied to skin. It is a common ingredient of many liniments.

    Jones, L.M., et al. Veterinary Pharmacology & Therapeutics. 4th ed. Ames: Iowa State University Press, 1977., p. 414

    MEDICATION (VET): /Camphor/ ... As a steam inhalant has been popular in respiratory diseases of horses and poultry. Orally, it has been popular in antiferment and carminative mixtures for calf scours, and in expectorant mixtures.

    Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 74

    For more Therapeutic Uses (Complete) data for CAMPHOR (10 total), please visit the HSDB record page.

    4.2 Drug Warning

    Keep pharmaceutical preparations and moth-repellents out of the reach of children and irresponsible people. Label camphorated oil appropriately to avoid mistaking it for castor oil and cough syrups. Do not place camphor ointments into infants' nostrils. Do not use the rubefacient on abraded skin.

    IPCS; Poisons Information Monograph 095: Camphor. (Date of last update: May 1989). Available from, as of June 30, 2014: https://www.inchem.org/documents/pims/pharm/camphor.htm#SectionTitle:1.5%20Brand%20names,%20Trade%20na

    Camphor and camphor containing products should be avoided in children who have a history of febrile convulsions or other predisposing factors for convulsions.

    National Poisons Information Service Center, United Kingdom; Poisons Information Monograph: Camphor. (March 1996). Available from, as of June 30, 2014: https://www.inchem.org/documents/ukpids/ukpids/ukpid19.htm

    Camphor should not be applied to the nostrils of infants even in small quantities, as this may cause immediate collapse.

    SWEETMAN, S.C. (ed.) Martindale-The Complete Drug Reference. 36th ed. London: The Pharmaceutical Press, 2009., p. 2273

    The UK Committee on the Review of Medicines recommended that camphor should not be included in products intended for the treatment of hepatic and biliary disorders, gallstones, colic, renal disorders, urinary tract infections, or ureteral stones. The use of camphor parenterally or as irrigants was considered undesirable due to the associated safety hazard.

    SWEETMAN, S.C. (ed.) Martindale-The Complete Drug Reference. 36th ed. London: The Pharmaceutical Press, 2009., p. 2273

    For more Drug Warnings (Complete) data for CAMPHOR (11 total), please visit the HSDB record page.

    4.3 Minimum/Potential Fatal Human Dose

    ...fatalities in children have been recorded from 1g.

    SWEETMAN, S.C. (ed.) Martindale-The Complete Drug Reference. 36th ed. London: The Pharmaceutical Press, 2009., p. 2273

    ...The literature from 1964-1983 /was reviewed/, and... the mean dose ingested by patients with major symptoms /was/ 124 mg/kg, with the mean dose in fatal cases being 199 mg/kg. /It was/... suggested, based on /the/ analysis of these figures, that patients ingesting <10 mg/kg of camphor and displaying no symptoms required no treatment. Adults have survived ingestions of up to 42 g, but usually doses in excess of 2 g produce dangerous effects. Fatal doses in children have ranged from 0.7-1.0 g.

    National Poisons Information Service Center, United Kingdom; Poisons Information Monograph: Camphor. (March 1996). Available from, as of June 30, 2014: https://www.inchem.org/documents/ukpids/ukpids/ukpid19.htm

    Dosages exceeding 2.0 grams have been reported to be /CNS depressant/ and may cause convulsions, delirium, hallucinations, and death.

    McGuffin M, Hobbs C et al., eds; American Herbal Products Association's Botanical Safety Handbook. p. 31 (1997)

    5 Pharmacology and Biochemistry
    5.1 MeSH Pharmacological Classification

    Anti-Infective Agents, Local

    Substances used on humans and other animals that destroy harmful microorganisms or inhibit their activity. They are distinguished from DISINFECTANTS, which are used on inanimate objects. (See all compounds classified as Anti-Infective Agents, Local.)

    5.2 Absorption, Distribution and Excretion

    Camphor is rapidly absorbed from the mucous membranes and the gastrointestinal tract. ... It is also absorbed through inhalation, through dermal application, and by nasal instillation.

    Ford MD, Delaney KA, Ling LJ, Erickson T; Clinical Toxicology. W.B. Saunders Company., Philadelphia, PA. 2001, p. 339

    ... after camphor ingestion by mothers ... camphor was detectable in maternal blood 15 min after ingestion, but not after 8 hr. At delivery 36 hr later ... it was present in amnionic fluid, cord and fetal blood and fetal brain, liver and kidneys.

    Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. III-85

    Alimentary absorption of pure camphor, or of alcohol solution ... is quite rapid, but from the oil preparation absorption is constant. Camphor is ... slowly absorbed from sc or im depots.

    Thienes, C., and T.J. Haley. Clinical Toxicology. 5th ed. Philadelphia: Lea and Febiger, 1972., p. 16

    Absorbed camphor is mainly eliminated as the oxidized camphorol in the urine, although some appears in the breath, sweat, and feces.

    Rossoff, I.S. Handbook of Veterinary Drugs. New York: Springer Publishing Company, 1974., p. 74

    For more Absorption, Distribution and Excretion (Complete) data for CAMPHOR (7 total), please visit the HSDB record page.

    5.3 Metabolism/Metabolites

    In the liver microsomes of female mice, two induction phases during inhalation of DL-camphor were found. During the first 24 hr the apparent molar activity of the ethylumbelliferone dealkylase decreased. In the second phase, the molar ethylumbelliferone dealkylase activity was constant.

    Mohn G; Different phases of hydroxylase induction in liver microsomes of female mice during inhalation of cyclohexane and D,L-camphor; Microsomes Drug Oxid, Proc Int Symp, 3rd: 59-66 (1977)

    The metabolism of (+)-camphor and (-)-camphor was investigated in rabbits after administration /through/ stomach tube; metabolites of (+)-camphor were (+)-borneol, (+)-5-endo-hydroxycamphor, and (+)-3-endohydroxycamphor.

    ROBERTSON JS, HUSSAIN M; METABOLISM OF CAMPHORS AND RELATED COMPOUNDS; BIOCHEM J 113 (1): 57-65 (1969)

    Camphor is rapidly oxidized to campherols (2-hydroxycamphor and 3-hydroxycamphor), and then conjugated in the liver to the glucuronide form. Camphor-related metabolites are relatively fat-soluble and may accumulate in fatty tissue.

    IPCS; Poisons Information Monograph 095: Camphor. (Date of last update:May 1989). Available from, as of June 30, 2014: https://www.inchem.org/documents/pims/pharm/camphor.htm#SectionTitle:1.5%20Brand%20names,%20Trade%20na

    5.4 Biological Half-Life

    167 minutes (200 mg camphor ingested alone); 93 minutes (200 mg camphor ingested with a solvent - Tween 80).

    National Poisons Information Service Center, United Kingdom; Poisons Information Monograph: Camphor. (March 1996). Available from, as of June 30, 2014: https://www.inchem.org/documents/ukpids/ukpids/ukpid19.htm

    5.5 Mechanism of Action

    Camphor is a naturally occurring compound that is used as a major active ingredient of balms and liniments supplied as topical analgesics. ... Capsaicin and menthol, two other topically applied agents widely used for similar purposes, are known to excite and desensitize sensory nerves by acting on two members of transient receptor potential (TRP) channel superfamily: heat-sensitive TRP vanilloid subtype 1 (TRPV1) and cold-sensitive TRP channel M8, respectively. Camphor has recently been shown to activate TRPV3, and here /investigators/ show that camphor also activates heterologously expressed TRPV1, requiring higher concentrations than capsaicin. Activation was enhanced by phospholipase C-coupled receptor stimulation mimicking inflamed conditions. Similar camphor-activated TRPV1-like currents were observed in isolated rat DRG neurons and were strongly potentiated after activation of protein kinase C with phorbol-12-myristate-13-acetate. Camphor activation of rat TRPV1 was mediated by distinct channel regions from capsaicin, as indicated by camphor activation in the presence of the competitive inhibitor capsazepine and in a capsaicin-insensitive point mutant. Camphor did not activate the capsaicin-insensitive chicken TRPV1. TRPV1 desensitization is believed to contribute to the analgesic actions of capsaicin. /The authors/ found that, although camphor activates TRPV1 less effectively, camphor application desensitized TRPV1 more rapidly and completely than capsaicin. Conversely, TRPV3 current sensitized after repeated camphor applications, which is inconsistent with the analgesic role of camphor. /Investigators/ also found that camphor inhibited several other related TRP channels, including ankyrin-repeat TRP 1 (TRPA1). The camphor-induced desensitization of TRPV1 and block of TRPA1 may underlie the analgesic effects of camphor.

    PMID:16192383 Xu H et al; J Neurosci. 25(39):8924-37 (2005).

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    03-Jan-2022
    30-Sep-2025
    KGS
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    ABOUT THIS PAGE

    Looking for 76-22-2 / Camphor API manufacturers, exporters & distributors?

    Camphor manufacturers, exporters & distributors 1

    66

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

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

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

    API | Excipient name

    Camphor

    Synonyms

    76-22-2, 2-camphanone, Dl-camphor, (+/-)-camphor, 2-bornanone, 1,7,7-trimethylbicyclo[2.2.1]heptan-2-one

    Cas Number

    76-22-2

    About Camphor

    A bicyclic monoterpene ketone found widely in plants, especially CINNAMOMUM CAMPHORA. It is used topically as a skin antipruritic and as an anti-infective agent.

    0-07-00-00135 (Beilstein Handbook Reference) Manufacturers

    A 0-07-00-00135 (Beilstein Handbook Reference) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0-07-00-00135 (Beilstein Handbook Reference), including repackagers and relabelers. The FDA regulates 0-07-00-00135 (Beilstein Handbook Reference) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    0-07-00-00135 (Beilstein Handbook Reference) Suppliers

    A 0-07-00-00135 (Beilstein Handbook Reference) supplier is an individual or a company that provides 0-07-00-00135 (Beilstein Handbook Reference) active pharmaceutical ingredient (API) or 0-07-00-00135 (Beilstein Handbook Reference) finished formulations upon request. The 0-07-00-00135 (Beilstein Handbook Reference) suppliers may include 0-07-00-00135 (Beilstein Handbook Reference) API manufacturers, exporters, distributors and traders.

    click here to find a list of 0-07-00-00135 (Beilstein Handbook Reference) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

    0-07-00-00135 (Beilstein Handbook Reference) USDMF

    A 0-07-00-00135 (Beilstein Handbook Reference) DMF (Drug Master File) is a document detailing the whole manufacturing process of 0-07-00-00135 (Beilstein Handbook Reference) active pharmaceutical ingredient (API) in detail. Different forms of 0-07-00-00135 (Beilstein Handbook Reference) DMFs exist exist since differing nations have different regulations, such as 0-07-00-00135 (Beilstein Handbook Reference) USDMF, ASMF (EDMF), JDMF, CDMF, etc.

    A 0-07-00-00135 (Beilstein Handbook Reference) DMF submitted to regulatory agencies in the US is known as a USDMF. 0-07-00-00135 (Beilstein Handbook Reference) USDMF includes data on 0-07-00-00135 (Beilstein Handbook Reference)'s chemical properties, information on the facilities and procedures used, and details about packaging and storage. The 0-07-00-00135 (Beilstein Handbook Reference) USDMF is kept confidential to protect the manufacturer’s intellectual property.

    click here to find a list of 0-07-00-00135 (Beilstein Handbook Reference) suppliers with USDMF on PharmaCompass.

    0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) Drug Master File in Japan (0-07-00-00135 (Beilstein Handbook Reference) JDMF) empowers 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) JDMF during the approval evaluation for pharmaceutical products. At the time of 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) suppliers with JDMF on PharmaCompass.

    0-07-00-00135 (Beilstein Handbook Reference) CEP

    A 0-07-00-00135 (Beilstein Handbook Reference) CEP of the European Pharmacopoeia monograph is often referred to as a 0-07-00-00135 (Beilstein Handbook Reference) Certificate of Suitability (COS). The purpose of a 0-07-00-00135 (Beilstein Handbook Reference) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 0-07-00-00135 (Beilstein Handbook Reference) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 0-07-00-00135 (Beilstein Handbook Reference) to their clients by showing that a 0-07-00-00135 (Beilstein Handbook Reference) CEP has been issued for it. The manufacturer submits a 0-07-00-00135 (Beilstein Handbook Reference) CEP (COS) as part of the market authorization procedure, and it takes on the role of a 0-07-00-00135 (Beilstein Handbook Reference) CEP holder for the record. Additionally, the data presented in the 0-07-00-00135 (Beilstein Handbook Reference) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 0-07-00-00135 (Beilstein Handbook Reference) DMF.

    A 0-07-00-00135 (Beilstein Handbook Reference) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) suppliers with CEP (COS) on PharmaCompass.

    0-07-00-00135 (Beilstein Handbook Reference) WC

    A 0-07-00-00135 (Beilstein Handbook Reference) written confirmation (0-07-00-00135 (Beilstein Handbook Reference) WC) is an official document issued by a regulatory agency to a 0-07-00-00135 (Beilstein Handbook Reference) manufacturer, verifying that the manufacturing facility of a 0-07-00-00135 (Beilstein Handbook Reference) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting 0-07-00-00135 (Beilstein Handbook Reference) APIs or 0-07-00-00135 (Beilstein Handbook Reference) finished pharmaceutical products to another nation, regulatory agencies frequently require a 0-07-00-00135 (Beilstein Handbook Reference) WC (written confirmation) as part of the regulatory process.

    click here to find a list of 0-07-00-00135 (Beilstein Handbook Reference) suppliers with Written Confirmation (WC) on PharmaCompass.

    0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) as an active pharmaceutical ingredient (API).

    Finished drug products

    The FDA updates the NDC directory daily. The NDC numbers for 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 0-07-00-00135 (Beilstein Handbook Reference) NDC to their finished compounded human drug products, they may choose to do so.

    click here to find a list of 0-07-00-00135 (Beilstein Handbook Reference) suppliers with NDC on PharmaCompass.

    0-07-00-00135 (Beilstein Handbook Reference) GMP

    0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) 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 0-07-00-00135 (Beilstein Handbook Reference) GMP manufacturer or 0-07-00-00135 (Beilstein Handbook Reference) GMP API supplier for your needs.

    0-07-00-00135 (Beilstein Handbook Reference) CoA

    A 0-07-00-00135 (Beilstein Handbook Reference) CoA (Certificate of Analysis) is a formal document that attests to 0-07-00-00135 (Beilstein Handbook Reference)'s compliance with 0-07-00-00135 (Beilstein Handbook Reference) specifications and serves as a tool for batch-level quality control.

    0-07-00-00135 (Beilstein Handbook Reference) CoA mostly includes findings from lab analyses of a specific batch. For each 0-07-00-00135 (Beilstein Handbook Reference) 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.

    0-07-00-00135 (Beilstein Handbook Reference) may be tested according to a variety of international standards, such as European Pharmacopoeia (0-07-00-00135 (Beilstein Handbook Reference) EP), 0-07-00-00135 (Beilstein Handbook Reference) JP (Japanese Pharmacopeia) and the US Pharmacopoeia (0-07-00-00135 (Beilstein Handbook Reference) 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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