DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories
02 1Granules India Limited
03 1Cdymax
04 1Cipla
05 1Formosa Laboratories
06 1Hetero Drugs
07 1Intas Pharmaceuticals
08 1Kekule Pharma
09 1Laurus Labs
10 1MSN Laboratories
11 1Medichem S.A
12 1Signa S.A. de C.V.
13 1Sun Pharmaceutical Industries Limited
14 1Blank
DRL 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 : 35732
Submission : 2021-03-31
Status :
Type : II
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36037
Submission : 2021-06-30
Status :
Type : II
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PharmaCompass offers a list of Pazopanib 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 Pazopanib Hydrochloride manufacturer or Pazopanib Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pazopanib Hydrochloride manufacturer or Pazopanib Hydrochloride supplier.
PharmaCompass also assists you with knowing the Pazopanib Hydrochloride API Price utilized in the formulation of products. Pazopanib Hydrochloride API Price is not always fixed or binding as the Pazopanib Hydrochloride Price is obtained through a variety of data sources. The Pazopanib Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A X3177 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of X3177, including repackagers and relabelers. The FDA regulates X3177 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. X3177 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A X3177 supplier is an individual or a company that provides X3177 active pharmaceutical ingredient (API) or X3177 finished formulations upon request. The X3177 suppliers may include X3177 API manufacturers, exporters, distributors and traders.
click here to find a list of X3177 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A X3177 DMF (Drug Master File) is a document detailing the whole manufacturing process of X3177 active pharmaceutical ingredient (API) in detail. Different forms of X3177 DMFs exist exist since differing nations have different regulations, such as X3177 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A X3177 DMF submitted to regulatory agencies in the US is known as a USDMF. X3177 USDMF includes data on X3177's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The X3177 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of X3177 suppliers with USDMF on PharmaCompass.
We have 13 companies offering X3177
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