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01 1Seqens

02 1Dr. Reddy's Laboratories

03 1Neuland Laboratories

04 1USV Private Limited

05 2TAPI Technology & API Services

06 1ALP Pharm

07 1Aurobindo Pharma Limited

08 2Catalent Pharma Solutions

09 1Cipla

10 1Emcure Pharmaceuticals

11 1Glenmark Pharmaceuticals

12 1Helsinn Advanced Synthesis

13 1Kyongbo Pharmaceutical Co., Ltd

14 1Lianyungang Runzhong Pharmaceutical Co Ltd

15 1MSN Laboratories

16 1Qilu Pharmaceutical

17 1RANBAXY LABORATORIES LIMITED

18 1Rolabo Outsourcing

19 1Tyche Industries Ltd

20 1Wockhardt

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PharmaCompass

01

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSeqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

GDUFA

DMF Review : Complete

Rev. Date : 2013-07-08

Pay. Date : 2013-01-16

DMF Number : 24798

Submission : 2011-03-23

Status : Active

Type : II

Seqens Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 23590

Submission : 2010-03-01

Status : Active

Type : II

Dr Reddy Company Banner

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNeuland Laboratories- A dedicated 100% API provider.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 21123

Submission : 2007-12-11

Status : Active

Type : II

Neuland

04

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothUSV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.

GDUFA

DMF Review : Complete

Rev. Date : 2015-12-17

Pay. Date : 2015-09-28

DMF Number : 28088

Submission : 2015-09-29

Status : Active

Type : II

USV Private Limited

05

  • fda
  • EDQM
  • WHO-GMP

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

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 21749

Submission : 2008-07-01

Status : Active

Type : II

TAPI Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

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

GDUFA

DMF Review : Complete

Rev. Date : 2013-04-23

Pay. Date : 2012-11-09

DMF Number : 23332

Submission : 2009-12-03

Status : Active

Type : II

TAPI Company Banner

10

PharmaVenue
Not Confirmed

10

PharmaVenue
Not Confirmed

GDUFA

DMF Review : Complete

Rev. Date : 2014-05-20

Pay. Date : 2014-03-10

DMF Number : 24497

Submission : 2010-12-23

Status : Active

Type : II

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Palonosetron Hydrochloride Manufacturers

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

Palonosetron Hydrochloride Suppliers

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

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

Palonosetron Hydrochloride USDMF

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

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

click here to find a list of Palonosetron 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.