01 1M/s Pride Drugs & Pharma (P) Ltd
02 1M/sChaitanya Biologicals Pvt Ltd
03 1M/sChaitanya Biologicals Pvt ltd
01 1Iron Hydroxide Polymaltose Complex 30-34% IH/ Iron Protein Succinate IH/Iron hydroxide Polysachharide IH
02 1Iron Hydroxide Polymaltose IH
03 1iron hydroxide polymaltose/ Iron protein succinylate
01 1WC-0449
02 1WC-0449A1
03 1WC-0490A2
01 3India
Date of Issue : 2022-04-05
Valid Till : 2025-07-28
Written Confirmation Number : WC-0449A1
Address of the Firm : 75/2 National Highway No 6, Malkapur Dist. Buldana Malkapur 433 101
iron hydroxide polymaltose/ Iron protein succinylate
Date of Issue : 2019-07-29
Valid Till : 2022-07-28
Written Confirmation Number : WC-0449
Address of the Firm : 75/2 National Highway No 6 Malkapur
Date of Issue : 2021-01-08
Valid Till : 2025-01-08
Written Confirmation Number : WC-0490A2
Address of the Firm : Block No 63, Bileshwarpura, P.O Chhatral,\r\nKalol-Mehsana Highway, Gandhinagar-...
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PharmaCompass offers a list of Iron III Hydroxide Polymaltose Complex 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 Iron III Hydroxide Polymaltose Complex manufacturer or Iron III Hydroxide Polymaltose Complex supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Iron III Hydroxide Polymaltose Complex manufacturer or Iron III Hydroxide Polymaltose Complex supplier.
PharmaCompass also assists you with knowing the Iron III Hydroxide Polymaltose Complex API Price utilized in the formulation of products. Iron III Hydroxide Polymaltose Complex API Price is not always fixed or binding as the Iron III Hydroxide Polymaltose Complex Price is obtained through a variety of data sources. The Iron III Hydroxide Polymaltose Complex Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Intrafer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Intrafer, including repackagers and relabelers. The FDA regulates Intrafer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Intrafer 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 Intrafer manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Intrafer supplier is an individual or a company that provides Intrafer active pharmaceutical ingredient (API) or Intrafer finished formulations upon request. The Intrafer suppliers may include Intrafer API manufacturers, exporters, distributors and traders.
click here to find a list of Intrafer suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Intrafer written confirmation (Intrafer WC) is an official document issued by a regulatory agency to a Intrafer manufacturer, verifying that the manufacturing facility of a Intrafer active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Intrafer APIs or Intrafer finished pharmaceutical products to another nation, regulatory agencies frequently require a Intrafer WC (written confirmation) as part of the regulatory process.
click here to find a list of Intrafer suppliers with Written Confirmation (WC) on PharmaCompass.
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