Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
01 1M/s Honour Lab Limited
02 1M/s Vasudha Pharma Chem Limited
03 1M/sSionc Pharmaceuticals Pvt ltd
01 3Diatrizoate Meglumine USP
01 1WC-0183
02 1WC-0273
03 1WC-0362
01 3India
Honour is a leading global CDMO and specialty chemicals manufacturer with seven world-class sites delivering quality-driven solutions.
Date of Issue : 2023-11-28
Valid Till : 2025-05-05
Written Confirmation Number : WC-0362
Address of the Firm : Plot No:4, Hetero Infrastructure SEZ Ltd.,\nNarasapuram, Visakhapatnam-531081,\n...
Date of Issue : 2023-11-15
Valid Till : 2026-05-11
Written Confirmation Number : WC-0273
Address of the Firm : Plot No: 34A, Road No: 1, Jawaharlal Nehru Pharma City, Thanam Village, Parawada...
Date of Issue : 2022-06-15
Valid Till : 2025-07-14
Written Confirmation Number : WC-0183
Address of the Firm : Unit-ll,PlotNo.79,Jawaharlal NehruPharmaCity, Thanam Village, Parawada Mandal, A...
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PharmaCompass offers a list of Diatrizoate Meglumine 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 Diatrizoate Meglumine manufacturer or Diatrizoate Meglumine supplier for your needs.
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PharmaCompass also assists you with knowing the Diatrizoate Meglumine API Price utilized in the formulation of products. Diatrizoate Meglumine API Price is not always fixed or binding as the Diatrizoate Meglumine Price is obtained through a variety of data sources. The Diatrizoate Meglumine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cystographin Dilute manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cystographin Dilute, including repackagers and relabelers. The FDA regulates Cystographin Dilute manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cystographin Dilute 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 Cystographin Dilute supplier is an individual or a company that provides Cystographin Dilute active pharmaceutical ingredient (API) or Cystographin Dilute finished formulations upon request. The Cystographin Dilute suppliers may include Cystographin Dilute API manufacturers, exporters, distributors and traders.
click here to find a list of Cystographin Dilute suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cystographin Dilute written confirmation (Cystographin Dilute WC) is an official document issued by a regulatory agency to a Cystographin Dilute manufacturer, verifying that the manufacturing facility of a Cystographin Dilute active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cystographin Dilute APIs or Cystographin Dilute finished pharmaceutical products to another nation, regulatory agencies frequently require a Cystographin Dilute WC (written confirmation) as part of the regulatory process.
click here to find a list of Cystographin Dilute suppliers with Written Confirmation (WC) on PharmaCompass.
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