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List of NDC API details of Lurasidone Active Pharmaceutical Ingredient listed on PharmaCompass.com

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Flag India
Digital Content Digital Content
Lurasidone Hydrochloride
POWDER (3kg/3kg)
BULK INGREDIENT
42765-009
2020-06-22
2024-12-31
Flag U.S.A
Digital Content Digital Content
Lurasidone HCl
POWDER (1kg/kg)
BULK INGREDIENT
49812-0270
2014-01-01
2024-12-31
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Digital Content Digital Content
Lurasidone Hydrochloride API
POWDER (1kg/kg)
BULK INGREDIENT
55111-957
2013-03-22
2024-12-31
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Lurasidone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
58032-2024
2016-07-09
2024-12-31
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URL Supplier Web Content
LURASIDONE HYDROCHLORIDE
POWDER (25kg/25kg)
BULK INGREDIENT FOR ...
17373-1185
2012-05-04
2024-12-31
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Lurasidone HCl
POWDER (50kg/50kg)
BULK INGREDIENT
65862-950
2024-01-11
2025-12-31
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lurasidone hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
66039-897
2013-07-26
2024-12-31
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Lurasidone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
65977-0103
2010-10-28
2024-12-31
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Lurasidone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
69011-0004
2019-09-04
2024-12-31
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lurasidone hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
65372-1192
2017-03-20
2024-12-31
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Lurasidone
POWDER (1kg/kg)
BULK INGREDIENT
50370-0036
2010-04-26
2024-12-31
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Lurasidone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
50370-0033
2012-04-19
2024-12-31
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Lurasidone Hydrochloride
POWDER (25kg/25kg)
BULK INGREDIENT
65085-0053
2018-11-19
2024-12-31
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LURASIDONE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
46016-3672
2013-11-29
2024-12-31
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LURASIDONE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
46016-3671
2013-11-29
2024-12-31
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Lurasidone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
66583-0516
2010-10-01
2024-12-31
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LURASIDONE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
72643-031
2022-12-30
2024-12-31
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lurasidone hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
38217-0010
2010-10-28
2024-12-31
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Lurasidone hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
53747-058
2015-03-31
2024-12-31
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LURASIDONE HYDROCHLORIDE
POWDER (1kg/kg)
BULK INGREDIENT
65015-843
2015-01-28
2024-12-31
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Lurasidone Hydrochloride
POWDER (1kg/kg)
BULK INGREDIENT
76072-1007
2017-06-05
2024-12-31
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  • TABLET;ORAL - 120MG
  • TABLET;ORAL - 20MG
  • TABLET;ORAL - 40MG
  • TABLET;ORAL - 60MG
  • TABLET;ORAL - 80MG

Looking for 367514-88-3 / Lurasidone API manufacturers, exporters & distributors?

Lurasidone manufacturers, exporters & distributors 1

18

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

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

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

API | Excipient name

Lurasidone

Synonyms

Lurasidone hcl, 367514-88-3, Latuda, Sm-13496, Lurasidone hydrochloride [usan], Sm 13496

Cas Number

367514-88-3

Unique Ingredient Identifier (UNII)

O0P4I5851I

About Lurasidone

A thiazole derivative and atypical ANTIPSYCHOTIC AGENT that functions as a DOPAMINE D2 RECEPTOR ANTAGONIST; SEROTONIN 5-HT2 RECEPTOR ANTAGONIST, serotonin 5-HT7 receptor antagonist, and antagonist of the adrenergic 2A and 2C receptors, as well as a partial SEROTONIN 5-HT1A RECEPTOR AGONIST. It is used in the treatment of SCHIZOPHRENIA and BIPOLAR DISORDER.

Lurasidone Manufacturers

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

Lurasidone Suppliers

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

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

Lurasidone 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 Lurasidone as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Lurasidone suppliers with NDC on PharmaCompass.

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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