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01 1Metrochem API Private Limited

02 1Veranova

03 1Cohance Lifesciences

04 1Dr. Reddy's Laboratories

05 1Neuland Laboratories

06 1TAPI Technology & API Services

07 1ALP Pharm

08 1Alembic Pharmaceuticals Limited

09 1Alkem Laboratories

10 1Amsa Spa

11 1Apotex Pharmachem

12 1Aurobindo Pharma Limited

13 1Biocon

14 1Glenmark Life Sciences

15 1Hetero Drugs

16 1Hisun Pharmaceutical Nantong

17 1Intas Pharmaceuticals

18 1Jubilant Generics

19 1Lee Pharma

20 1Lupin Ltd

21 2MSN Laboratories

22 1Macleods Pharmaceuticals Limited

23 1Micro Labs Limited

24 1Piramal Pharma Solutions

25 1Procos

26 1Raks Pharma

27 1Recipharm AB

28 1Solara Active Pharma Sciences

29 1Sumitomo Pharma

30 1Sun Pharmaceutical Industries Limited

31 1Torrent Pharmaceuticals Limited

32 1Unichem Laboratories Limited

33 1Viatris

34 1Zydus Lifesciences

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PharmaCompass

01

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMetrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 34756

Submission : 2020-07-14

Status : Active

Type : II

Metrochem

02

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothVeranova: A CDMO that manages complexity with confidence.

GDUFA

DMF Review : Complete

Rev. Date : 2020-04-07

Pay. Date : 2019-12-03

DMF Number : 34255

Submission : 2020-01-31

Status : Active

Type : II

Veranova

03

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 31801

Submission : 2017-06-06

Status : Active

Type : II

Cohance

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

GDUFA

DMF Review : Complete

Rev. Date : 2014-10-06

Pay. Date : 2014-08-05

DMF Number : 26700

Submission : 2013-03-22

Status : Active

Type : II

Dr Reddy Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNeuland Laboratories- A dedicated 100% API provider.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 29794

Submission : 2016-05-07

Status : Active

Type : II

Neuland

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

GDUFA

DMF Review : Complete

Rev. Date : 2014-08-01

Pay. Date : 2014-04-08

DMF Number : 28178

Submission : 2014-04-28

Status : Active

Type : II

TAPI Company Banner

07

PharmaVenue
Not Confirmed

08

PharmaVenue
Not Confirmed

Lurasidone Hydrochloride Manufacturers

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

Lurasidone Hydrochloride Suppliers

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

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

Lurasidone Hydrochloride USDMF

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

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

click here to find a list of Lurasidone Hydrochloride suppliers with USDMF 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.