Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
01 1Medichem S.A.
02 1AX Pharmaceutical Corp
03 1Aurobindo Pharma Limited
04 1Jubilant Pharmova Limited
05 2MYLAN LABORATORIES LIMITED
06 1Medisca Inc.
07 1ThermoFisher Scientific Cork
08 1Tianish Laboratories Private Limited
09 1Wanbury Limited
10 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
01 1PAROXETINE HYDROCHLORIDE (ANHYDROUS)
02 2PAROXETINE HYDROCHLORIDE (HEMIHYDRATE)
03 1PAROXETINE HYDROCHLORIDE HEMIHYDRATE
04 1Paroxetine Hydrochloride (Hemihydrate)
05 4Paroxetine Hydrochloride Hemihydrate
06 1paroxetine hydrochloride
07 1paroxetine hydrochloride (hemihydrate)
01 1Canada
02 1China
03 4India
04 1Spain
05 4U.S.A
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 53296-0057
Start Marketing Date : 2010-05-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 65862-382
Start Marketing Date : 2023-12-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 73377-051
Start Marketing Date : 2020-05-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 65372-1133
Start Marketing Date : 2009-03-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 38779-3316
Start Marketing Date : 2024-11-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 61187-005
Start Marketing Date : 2014-09-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 65015-741
Start Marketing Date : 2015-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE ANHYDROUS
NDC Package Code : 65015-742
Start Marketing Date : 2015-02-24
End Marketing Date : 2026-12-01
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 62350-0044
Start Marketing Date : 2018-12-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
PAROXETINE HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 64220-113
Start Marketing Date : 2008-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Paroxetine 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 Paroxetine Hydrochloride manufacturer or Paroxetine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Paroxetine Hydrochloride manufacturer or Paroxetine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Paroxetine Hydrochloride API Price utilized in the formulation of products. Paroxetine Hydrochloride API Price is not always fixed or binding as the Paroxetine Hydrochloride Price is obtained through a variety of data sources. The Paroxetine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Paroxetine Hydrochloride Anhydrous manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Paroxetine Hydrochloride Anhydrous, including repackagers and relabelers. The FDA regulates Paroxetine Hydrochloride Anhydrous manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Paroxetine Hydrochloride Anhydrous 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 Paroxetine Hydrochloride Anhydrous manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Paroxetine Hydrochloride Anhydrous supplier is an individual or a company that provides Paroxetine Hydrochloride Anhydrous active pharmaceutical ingredient (API) or Paroxetine Hydrochloride Anhydrous finished formulations upon request. The Paroxetine Hydrochloride Anhydrous suppliers may include Paroxetine Hydrochloride Anhydrous API manufacturers, exporters, distributors and traders.
click here to find a list of Paroxetine Hydrochloride Anhydrous 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 Paroxetine Hydrochloride Anhydrous as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Paroxetine Hydrochloride Anhydrous 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 Paroxetine Hydrochloride Anhydrous 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 Paroxetine Hydrochloride Anhydrous and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Paroxetine Hydrochloride Anhydrous NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Paroxetine Hydrochloride Anhydrous suppliers with NDC on PharmaCompass.
We have 10 companies offering Paroxetine Hydrochloride Anhydrous
Get in contact with the supplier of your choice:
