EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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01 1EUROAPI Germany GmbH
02 1Dr.Reddy's Laboratoriees Limited
03 1Aarti Pharmalabs Limited
04 1Neuland Laboratories Limited
05 1Aurobindo Pharma Limited
06 1Cipla Ltd.
07 1Hetero Labs Limited
08 1Honour Lab Limited
09 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
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01 9Ramipril
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01 1China
02 1France
03 7India
NDC Package Code : 82348-101
Start Marketing Date : 2010-07-20
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 : 55111-057
Start Marketing Date : 2002-10-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-0300
Start Marketing Date : 2016-08-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58032-0123
Start Marketing Date : 2017-12-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-320
Start Marketing Date : 2024-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7573
Start Marketing Date : 2016-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0004
Start Marketing Date : 1991-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69037-0051
Start Marketing Date : 1991-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64220-118
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 Ramipril 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 Ramipril manufacturer or Ramipril supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ramipril manufacturer or Ramipril supplier.
PharmaCompass also assists you with knowing the Ramipril API Price utilized in the formulation of products. Ramipril API Price is not always fixed or binding as the Ramipril Price is obtained through a variety of data sources. The Ramipril Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Naprix manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Naprix, including repackagers and relabelers. The FDA regulates Naprix manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Naprix 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 Naprix manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Naprix supplier is an individual or a company that provides Naprix active pharmaceutical ingredient (API) or Naprix finished formulations upon request. The Naprix suppliers may include Naprix API manufacturers, exporters, distributors and traders.
click here to find a list of Naprix 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 Naprix as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Naprix 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 Naprix 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 Naprix and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Naprix NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Naprix suppliers with NDC on PharmaCompass.
We have 9 companies offering Naprix
Get in contact with the supplier of your choice: