01 1M/s Aurore Pharmaceuticals Private limited
02 1M/s Azico Biophore India pvt Ltd
03 1M/s Gland Pharma Limited
04 1M/s. Innova Remedies Pvt. Ltd
01 1Levothyroxine Sodium BP/Ph.Eur
02 1Levothyroxine Sodium USP
03 1Levothyroxine Sodium USP/Ph.Eur
04 1Levothyroxine sodium USP/Ph.Eur
01 1WC-0119
02 1WC-0404
03 1WC-0427
04 1WC-0572
01 4India
Levothyroxine sodium USP/Ph.Eur
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm : Plot No. 35, 36, 38, 39, 40, 49, 50 & 51, Phase-IV, IDA, Jeedimetla, Medchal-Mal...
Levothyroxine Sodium USP/Ph.Eur
Date of Issue : 2023-11-15
Valid Till : 2026-11-14
Written Confirmation Number : WC-0404
Address of the Firm : Plot No. 40/A, Sy Nos. 13,15,16,51,52 & 182, J.N. Pharma city, Thanam Village, P...
Date of Issue : 2022-04-08
Valid Till : 2025-04-03
Written Confirmation Number : WC-0427
Address of the Firm : Plot No.49 & 50, J.N. Pharma City, Parawada (M), Visakhapatanam
Levothyroxine Sodium BP/Ph.Eur
Date of Issue : 2023-11-03
Valid Till : 2026-11-02
Written Confirmation Number : WC-0572
Address of the Firm : SurveyNo.338(P-38), NexttoMIDCindustrialarea, KHNo.:25/3,kanhan-Mansar Highway N...
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PharmaCompass also assists you with knowing the Levothyroxine Sodium API Price utilized in the formulation of products. Levothyroxine Sodium API Price is not always fixed or binding as the Levothyroxine Sodium Price is obtained through a variety of data sources. The Levothyroxine Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Synthroid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Synthroid, including repackagers and relabelers. The FDA regulates Synthroid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Synthroid 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 Synthroid supplier is an individual or a company that provides Synthroid active pharmaceutical ingredient (API) or Synthroid finished formulations upon request. The Synthroid suppliers may include Synthroid API manufacturers, exporters, distributors and traders.
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A Synthroid written confirmation (Synthroid WC) is an official document issued by a regulatory agency to a Synthroid manufacturer, verifying that the manufacturing facility of a Synthroid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Synthroid APIs or Synthroid finished pharmaceutical products to another nation, regulatory agencies frequently require a Synthroid WC (written confirmation) as part of the regulatory process.
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