Market Place
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations. 
X
Please Wait
Applying Filters...
01 Dr. Reddy's Laboratories (1)
02 Aarti Pharmalabs (2)
03 Neuland Laboratories (1)
04 Actavis Inc (1)
05 Apotex Pharmachem (1)
06 Aurobindo Pharma Limited (1)
07 Cipla (1)
08 Esteve Quimica (1)
09 Farmhispania (1)
10 Hetero Drugs (1)
11 Lupin Ltd (2)
12 Melody Healthcare Pvt Ltd (1)
13 RANBAXY LABORATORIES LIMITED (1)
14 SMS Pharmaceuticals (1)
15 Unimark Remedies Limited (1)
16 Zhejiang Huahai Pharmaceutical (1)
01 FH-113 (RAMIPRIL) (1)
02 RAMIPRIL (5)
03 RAMIPRIL USP (1)
04 RAMIPRIL USP (8)
05 RAMIPRIL USP (GRADE A) (1)
06 RAMIPRIL USP (PROCESS B) (1)
07 RAMIPRIL USP, GRADE II (1)
01 Canada (1)
02 China (1)
03 India (13)
04 Ireland (1)
05 Spain (2)
01 Active (11)
02 Inactive (7)
01 Complete (2)
02 Blank (16)
66
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 MolPort-001-736-571 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-736-571, including repackagers and relabelers. The FDA regulates MolPort-001-736-571 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-736-571 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 MolPort-001-736-571 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A MolPort-001-736-571 supplier is an individual or a company that provides MolPort-001-736-571 active pharmaceutical ingredient (API) or MolPort-001-736-571 finished formulations upon request. The MolPort-001-736-571 suppliers may include MolPort-001-736-571 API manufacturers, exporters, distributors and traders.
click here to find a list of MolPort-001-736-571 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A MolPort-001-736-571 DMF (Drug Master File) is a document detailing the whole manufacturing process of MolPort-001-736-571 active pharmaceutical ingredient (API) in detail. Different forms of MolPort-001-736-571 DMFs exist exist since differing nations have different regulations, such as MolPort-001-736-571 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A MolPort-001-736-571 DMF submitted to regulatory agencies in the US is known as a USDMF. MolPort-001-736-571 USDMF includes data on MolPort-001-736-571's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The MolPort-001-736-571 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of MolPort-001-736-571 suppliers with USDMF on PharmaCompass.
We have 16 companies offering MolPort-001-736-571
Get in contact with the supplier of your choice:
