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Chemistry

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Also known as: 136434-34-9, Duloxetine hcl, Cymbalta, (s)-duloxetine hydrochloride, Ariclaim, Xeristar
Molecular Formula
C18H20ClNOS
Molecular Weight
333.9  g/mol
InChI Key
BFFSMCNJSOPUAY-LMOVPXPDSA-N
FDA UNII
9044SC542W

Duloxetine Hydrochloride
A thiophene derivative and selective NEUROTRANSMITTER UPTAKE INHIBITOR for SEROTONIN and NORADRENALINE (SNRI). It is an ANTIDEPRESSIVE AGENT and ANXIOLYTIC, and is also used for the treatment of pain in patients with DIABETES MELLITUS and FIBROMYALGIA.
1 2D Structure

Duloxetine Hydrochloride

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(3S)-N-methyl-3-naphthalen-1-yloxy-3-thiophen-2-ylpropan-1-amine;hydrochloride
2.1.2 InChI
InChI=1S/C18H19NOS.ClH/c1-19-12-11-17(18-10-5-13-21-18)20-16-9-4-7-14-6-2-3-8-15(14)16;/h2-10,13,17,19H,11-12H2,1H3;1H/t17-;/m0./s1
2.1.3 InChI Key
BFFSMCNJSOPUAY-LMOVPXPDSA-N
2.1.4 Canonical SMILES
CNCCC(C1=CC=CS1)OC2=CC=CC3=CC=CC=C32.Cl
2.1.5 Isomeric SMILES
CNCC[C@@H](C1=CC=CS1)OC2=CC=CC3=CC=CC=C32.Cl
2.2 Other Identifiers
2.2.1 UNII
9044SC542W
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Cymbalta

2. Duloxetine

3. Duloxetine Ethanedioate (1:1), (+-)-isomer - T353987

4. Duloxetine Hcl

5. Duloxetine, (+)-isomer

6. Hcl, Duloxetine

7. Hydrochloride, Duloxetine

8. Ly 227942

9. Ly 248686

10. Ly-227942

11. Ly-248686

12. Ly227942

13. Ly248686

14. N-methyl-3-(1-naphthalenyloxy)-2-thiophenepropanamine

15. N-methyl-3-(1-naphthalenyloxy)-3-(2-thiophene)propanamide

2.3.2 Depositor-Supplied Synonyms

1. 136434-34-9

2. Duloxetine Hcl

3. Cymbalta

4. (s)-duloxetine Hydrochloride

5. Ariclaim

6. Xeristar

7. (s)-n-methyl-3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propan-1-amine Hydrochloride

8. Duloxetine Hydrochloride [usan]

9. Duloxetine Mylan

10. Duloxetine (hydrochloride)

11. Ly248686 Hcl

12. Ly-248686 Hcl

13. Nsc-759112

14. Cpd000469136

15. Duloxetine (as Hydrochloride)

16. Chebi:31526

17. (3s)-n-methyl-3-naphthalen-1-yloxy-3-thiophen-2-ylpropan-1-amine;hydrochloride

18. 9044sc542w

19. Yentreve (tn)

20. (+)-(s)-n-methyl-gamma-(1-naphthyloxy)-2-thiophenepropylamine Hydrochloride

21. Dsstox_cid_26443

22. Dsstox_rid_81618

23. Dsstox_gsid_46443

24. Duloxetine Boehringer Ingelheim

25. Methyl[3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propyl]amine Hydrochloride

26. (+)-(s)-n-methyl-.gamma.-(1-naphthyloxy)-2-thiophenepropylamine Hydrochloride

27. (s)-n-methyl-3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propan-1-amine Hcl

28. Smr000469136

29. Dulane 20

30. Cas-136434-34-9

31. Ncgc00164559-01

32. C18h19nos.hcl

33. Unii-9044sc542w

34. Ly 248686 Hcl

35. Cymbalta (tn)

36. Duloxetina Cloridrato

37. Duloxetine Hydrochlorise

38. Duloxetine Lilly

39. Cloridrato De Duloxetina

40. Clorhidrato De Duloxetina

41. Chlorhydrate De Duloxetine

42. Duloxetine Hcl (cymbalta)

43. Mls001401452

44. Mls006010054

45. (s)-duloxetine (hydrochloride)

46. Duloxetine Hydrochloride- Bio-x

47. Chembl1200328

48. Dtxsid9046443

49. Duloxetine Hydrochloride Solution

50. Duloxetine For System Suitability

51. Hy-b0161a

52. Pharmakon1600-01505387

53. Ly-248686 Hydrochloride

54. Amy12420

55. Duloxetine Hydrochloride (jan/usp)

56. Tox21_112188

57. Ac-924

58. Duloxetine Hydrochloride [mi]

59. Mfcd06407958

60. Nsc744012

61. Nsc759112

62. S2084

63. Duloxetine Hydrochloride [jan]

64. (3s)-n-methyl-3-(1-naphthyloxy)-3-(2-thienyl)propan-1-amine Hydrochloride

65. Akos016340453

66. Tox21_112188_1

67. Ccg-101106

68. Cs-1993

69. Ks-1168

70. Nc00356

71. Nsc 759112

72. Nsc-744012

73. (3s)-n-methyl-3-naphthalen-1-yloxy-3-thiophen-2-ylpropan-1-amine Hydrochloride

74. 2-thiophenepropanamine, N-methyl-gamma-(1-naphthalenyloxy)-, Hydrochloride, (gammas)-

75. 2-thiophenepropanamine, N-methyl-gamma-(1-naphthalenyloxy)-, Hydrochloride, (s)-

76. Duloxetine Hydrochloride [mart.]

77. Duloxetine Hydrochloride [usp-rs]

78. Duloxetine Hydrochloride [who-dd]

79. Ncgc00164559-03

80. (s)-(+)-duloxetine Hydrochloride

81. Bd165546

82. Ly-264453

83. D-170

84. D4223

85. Sw197393-3

86. Duloxetine Hydrochloride [orange Book]

87. (s)-duloxetine Hydrochloride, >=98% (hplc)

88. D01179

89. Duloxetine Hydrochloride [ep Monograph]

90. Duloxetine Hydrochloride [usp Monograph]

91. 434d349

92. Q-102508

93. Duloxetine Hydrochloride 1.0 Mg/ml In Methanol (as Free Base)

94. (+)-(s)-n-methyl-3-(1-naphthyloxy)-3-(2-thienyl)propanamine Hydrochloride

95. Duloxetine Hydrochloride, European Pharmacopoeia (ep) Reference Standard

96. (+)-(s)-n-methyl-3-(1-naphthyloxy)- 3-(2-thienyl)propanamine Hydrochloride

97. (3s)-n-methyl-3-(naphthalen-1-yloxy)-3-(2-thienyl)propan-1-amine Hydrochloride

98. (3s)-n-methyl-3-naphthalen-1-yloxy-3-thiophen-2-ylpropan-1-amin Hydrochloride.

99. (gammas)-2-thiophenepropanamine, N-methyl-gamma-(1-naphthalenyloxy)hydrochloride (1:1)

100. (gammas)-n-methyl-gamma-(1-naphthalenyloxy)-2-thiophenepropanamine Hydrochloride

101. (s)-(+)-n-methyl-3-(1-naphthalenyloxy)-3-(2-thienyl) Propanamine Hydrochloride

102. (s)-(+)-n-methyl-3-(1-naphthyloxy)-3-(2-thienyl)propylamine Hydrochloride

103. 2-thiophenepropanamine, N-methyl-.gamma.-(1-naphthalenyloxy)-, Hydrochloride, (s)-

104. Duloxetine For System Suitability, European Pharmacopoeia (ep) Reference Standard

105. Duloxetine Hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material

106. Duloxetine Hydrochloride, United States Pharmacopeia (usp) Reference Standard

2.4 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 333.9 g/mol
Molecular Formula C18H20ClNOS
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count3
Rotatable Bond Count6
Exact Mass333.0954131 g/mol
Monoisotopic Mass333.0954131 g/mol
Topological Polar Surface Area49.5 Ų
Heavy Atom Count22
Formal Charge0
Complexity312
Isotope Atom Count0
Defined Atom Stereocenter Count1
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Information
1 of 4  
Drug NameCymbalta
PubMed HealthDuloxetine (By mouth)
Drug ClassesAntidepressant, Central Nervous System Agent, Neuropathic Pain Agent
Drug LabelCymbalta (Duloxetine Delayed-Release Capsules) is a selective serotonin and norepinephrine reuptake inhibitor (SSNRI) for oral administration. Its chemical designation is (+)-( )- -methyl--(1-naphthyloxy)-2-thiophenepropylamine hydrochloride. The e...
Active IngredientDuloxetine hydrochloride
Dosage FormCapsule, delayed rel pellets
Routeoral; Oral
Strengtheq 30mg base; eq 20mg base; eq 60mg base
Market StatusPrescription
CompanyLilly

2 of 4  
Drug NameDuloxetine hydrochloride
Drug LabelCymbalta (Duloxetine Delayed-Release Capsules) is a selective serotonin and norepinephrine reuptake inhibitor (SSNRI) for oral administration. Its chemical designation is (+)-( )- -methyl--(1-naphthyloxy)-2-thiophenepropylamine hydrochloride. The e...
Active IngredientDuloxetine hydrochloride
Dosage FormCapsule, delayed rel pellets; Capsule, delayed release
Routeoral; Oral
Strengtheq 40mg base; 60mg; 30mg; eq 30mg base; eq 20mg base; eq 60mg base; 20mg
Market StatusTentative Approval; Prescription
CompanyWockhardt; Actavis Elizabeth; Breckenridge Pharm; Apotex; Alembic Pharms; Teva Pharms Usa; Aurobindo Pharma; Torrent Pharms; Zydus Pharms Usa; Lupin; Dr Reddys Labs; Sandoz; Sun Pharma Global; Impax Labs

3 of 4  
Drug NameCymbalta
PubMed HealthDuloxetine (By mouth)
Drug ClassesAntidepressant, Central Nervous System Agent, Neuropathic Pain Agent
Drug LabelCymbalta (Duloxetine Delayed-Release Capsules) is a selective serotonin and norepinephrine reuptake inhibitor (SSNRI) for oral administration. Its chemical designation is (+)-( )- -methyl--(1-naphthyloxy)-2-thiophenepropylamine hydrochloride. The e...
Active IngredientDuloxetine hydrochloride
Dosage FormCapsule, delayed rel pellets
Routeoral; Oral
Strengtheq 30mg base; eq 20mg base; eq 60mg base
Market StatusPrescription
CompanyLilly

4 of 4  
Drug NameDuloxetine hydrochloride
Drug LabelCymbalta (Duloxetine Delayed-Release Capsules) is a selective serotonin and norepinephrine reuptake inhibitor (SSNRI) for oral administration. Its chemical designation is (+)-( )- -methyl--(1-naphthyloxy)-2-thiophenepropylamine hydrochloride. The e...
Active IngredientDuloxetine hydrochloride
Dosage FormCapsule, delayed rel pellets; Capsule, delayed release
Routeoral; Oral
Strengtheq 40mg base; 60mg; 30mg; eq 30mg base; eq 20mg base; eq 60mg base; 20mg
Market StatusTentative Approval; Prescription
CompanyWockhardt; Actavis Elizabeth; Breckenridge Pharm; Apotex; Alembic Pharms; Teva Pharms Usa; Aurobindo Pharma; Torrent Pharms; Zydus Pharms Usa; Lupin; Dr Reddys Labs; Sandoz; Sun Pharma Global; Impax Labs

4.2 Drug Indication

- Treatment of major depressive disorder;

- Treatment of diabetic peripheral neuropathic pain;

- Treatment of generalised anxiety disorder;

- Duloxetine Mylan is indicated in adults.


Duloxetine Lilly is indicated in adults for:

- Treatment of major depressive disorder

- Treatment of diabetic peripheral neuropathic pain

- Treatment of generalised anxiety disorder

Duloxetine Lilly is indicated in adults.


Yentreve is indicated for women for the treatment of moderate to severe stress urinary incontinence (SUI).


Treatment of major depressive disorder.

Treatment of diabetic peripheral neuropathic pain.

Treatment of generalised anxiety disorder.

Cymbalta is indicated in adults.


Treatment of diabetic peripheral neuropathic pain.

Ariclaim is indicated in adults.


Treatment of diabetic peripheral neuropathic pain in adults.


Treatment of chronic pain, Treatment of diabetic neuropathic pain, Treatment of generalised anxiety disorder, Treatment of major depressive disorder, Treatment of stress urinary incontinence


5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

Antidepressive Agents

Mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several MONOAMINE OXIDASE INHIBITORS are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (ANTIDEPRESSIVE AGENTS, TRICYCLIC) also appear to act through brain catecholamine systems. A third group (ANTIDEPRESSIVE AGENTS, SECOND-GENERATION) is a diverse group of drugs including some that act specifically on serotonergic systems. (See all compounds classified as Antidepressive Agents.)


Analgesics

Compounds capable of relieving pain without the loss of CONSCIOUSNESS. (See all compounds classified as Analgesics.)


Serotonin and Noradrenaline Reuptake Inhibitors

Drugs that selectively block or suppress the plasma membrane transport of SEROTONIN and NORADRENALINE into axon terminals and are used as ANTIDEPRESSIVE AGENTS. (See all compounds classified as Serotonin and Noradrenaline Reuptake Inhibitors.)


Dopamine Agents

Any drugs that are used for their effects on dopamine receptors, on the life cycle of dopamine, or on the survival of dopaminergic neurons. (See all compounds classified as Dopamine Agents.)


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
Serotonin Uptake Inhibitors [MoA]; Serotonin and Norepinephrine Reuptake Inhibitor [EPC]; Norepinephrine Uptake Inhibitors [MoA]
5.3 ATC Code

N06AX21


N06AX21


N06AX21


N06AX21


N06AX21


N06AX21


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DULOXETINE HYDROCHLORIDE PH,EUR.","address":"ALEMBIC ROAD","city":"GUJARAT","supplier":"ZHEJIANG HUAHAI PHARMACEUTICAL CO","supplierCountry":"CHINA","foreign_port":"SHANGHAI","customer":"ALEMBIC PHARMACEUTICALS LTD","customerCountry":"INDIA","quantity":"126.57","actualQuantity":"126.57","unit":"KGS","unitRateFc":"165","totalValueFC":"21062.2","currency":"USD","unitRateINR":"14322","date":"29-Jul-2025","totalValueINR":"1812735.54","totalValueInUsd":"21062.2","indian_port":"Bombay Air","hs_no":"29349990","bill_no":"3561652","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"SHANGHAI","supplierAddress":"LTD.XUNQIAO LINHAI ZHEJIANG 317024 SDNF SDNF CHINA","customerAddress":"ALEMBIC ROAD"}]
07-Jan-2022
31-Jul-2025
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DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - ...DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - EQ 20MG BASE

USFDA APPLICATION NUMBER - 21427

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DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - ...DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - EQ 30MG BASE

USFDA APPLICATION NUMBER - 21427

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DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - ...DOSAGE - CAPSULE, DELAYED REL PELLETS;ORAL - EQ 60MG BASE

USFDA APPLICATION NUMBER - 21427

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ABOUT THIS PAGE

Looking for 136434-34-9 / Duloxetine Hydrochloride API manufacturers, exporters & distributors?

Duloxetine Hydrochloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Duloxetine Hydrochloride

Synonyms

136434-34-9, Duloxetine hcl, Cymbalta, (s)-duloxetine hydrochloride, Ariclaim, Xeristar

Cas Number

136434-34-9

Unique Ingredient Identifier (UNII)

9044SC542W

About Duloxetine Hydrochloride

A thiophene derivative and selective NEUROTRANSMITTER UPTAKE INHIBITOR for SEROTONIN and NORADRENALINE (SNRI). It is an ANTIDEPRESSIVE AGENT and ANXIOLYTIC, and is also used for the treatment of pain in patients with DIABETES MELLITUS and FIBROMYALGIA.

(S)-Duloxetine (hydrochloride) Manufacturers

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

(S)-Duloxetine (hydrochloride) Suppliers

A (S)-Duloxetine (hydrochloride) supplier is an individual or a company that provides (S)-Duloxetine (hydrochloride) active pharmaceutical ingredient (API) or (S)-Duloxetine (hydrochloride) finished formulations upon request. The (S)-Duloxetine (hydrochloride) suppliers may include (S)-Duloxetine (hydrochloride) API manufacturers, exporters, distributors and traders.

click here to find a list of (S)-Duloxetine (hydrochloride) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

(S)-Duloxetine (hydrochloride) USDMF

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

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

click here to find a list of (S)-Duloxetine (hydrochloride) suppliers with USDMF on PharmaCompass.

(S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) Drug Master File in Japan ((S)-Duloxetine (hydrochloride) JDMF) empowers (S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) JDMF during the approval evaluation for pharmaceutical products. At the time of (S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) suppliers with JDMF on PharmaCompass.

(S)-Duloxetine (hydrochloride) KDMF

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

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

After submitting a (S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) API can apply through the Korea Drug Master File (KDMF).

click here to find a list of (S)-Duloxetine (hydrochloride) suppliers with KDMF on PharmaCompass.

(S)-Duloxetine (hydrochloride) CEP

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

A (S)-Duloxetine (hydrochloride) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. (S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) suppliers with CEP (COS) on PharmaCompass.

(S)-Duloxetine (hydrochloride) WC

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

click here to find a list of (S)-Duloxetine (hydrochloride) suppliers with Written Confirmation (WC) on PharmaCompass.

(S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for (S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a (S)-Duloxetine (hydrochloride) NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of (S)-Duloxetine (hydrochloride) suppliers with NDC on PharmaCompass.

(S)-Duloxetine (hydrochloride) GMP

(S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) 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 (S)-Duloxetine (hydrochloride) GMP manufacturer or (S)-Duloxetine (hydrochloride) GMP API supplier for your needs.

(S)-Duloxetine (hydrochloride) CoA

A (S)-Duloxetine (hydrochloride) CoA (Certificate of Analysis) is a formal document that attests to (S)-Duloxetine (hydrochloride)'s compliance with (S)-Duloxetine (hydrochloride) specifications and serves as a tool for batch-level quality control.

(S)-Duloxetine (hydrochloride) CoA mostly includes findings from lab analyses of a specific batch. For each (S)-Duloxetine (hydrochloride) 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.

(S)-Duloxetine (hydrochloride) may be tested according to a variety of international standards, such as European Pharmacopoeia ((S)-Duloxetine (hydrochloride) EP), (S)-Duloxetine (hydrochloride) JP (Japanese Pharmacopeia) and the US Pharmacopoeia ((S)-Duloxetine (hydrochloride) 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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