Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
01 1Wavelength Enterprises LTD
02 1Dr.Reddy's Laboratories Limited
03 1Neuland Laboratories Limited
04 1USV Private Limited
05 1Aurobindo Pharma Limited
06 1Cipla Ltd.
07 1Emcure Pharmaceuticals Limited
08 1HAS Healthcare Advanced Synthesis SA
09 1MSN Laboratories Private Limited
10 1Qilu Pharmaceutical Co. Ltd.
11 1Rolabo Outsourcing S.L.
12 1TAPI Czech Industries s.r.o.
13 1TYCHE INDUSTRIES LIMITED
14 1Teva Czech Industries s.r.o
01 4PALONOSETRON HYDROCHLORIDE
02 10Palonosetron Hydrochloride
01 1China
02 1France
03 8India
04 1Israel
05 1Spain
06 1Switzerland
07 1Blank
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
NDC Package Code : 58175-0543
Start Marketing Date : 2008-02-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-914
Start Marketing Date : 2010-03-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58032-0135
Start Marketing Date : 2017-12-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62147-0218
Start Marketing Date : 2014-04-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7733
Start Marketing Date : 2014-05-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-846
Start Marketing Date : 2022-02-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54893-0013
Start Marketing Date : 2013-05-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63827-1011
Start Marketing Date : 2011-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-027
Start Marketing Date : 2022-01-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60862-003
Start Marketing Date : 2014-12-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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.
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.
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 Palonosetron Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Palonosetron Hydrochloride API and other APIs are published in this directory by the FDA.
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 Palonosetron 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.
The NDC directory also contains data on finished compounded human drug products that contain Palonosetron Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Palonosetron Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Palonosetron Hydrochloride suppliers with NDC on PharmaCompass.
We have 13 companies offering Palonosetron Hydrochloride
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