Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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01 1Syn-Tech Chem & Pharm Co., Ltd.
02 1M/s Medinex Laboratories Pvt Ltd
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01 1Epinephrine Bitartrate
02 1Epinephrine Bitartrate USP
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01 1TFDA-0002291
02 1WC-0279
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01 1India
02 1Taiwan
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Date of Issue : 2022-02-22
Valid Till : 2026-12-31
Written Confirmation Number : TFDA-0002291
Address of the Firm : No. 168, Kai Yuan Rd, Hsin-Ying, Tainan City 73055, Taiwan
Date of Issue : 2024-11-07
Valid Till : 2027-06-24
Written Confirmation Number : WC-0279
Address of the Firm : Plot No. 2 & 3, Sr No. 277/1, Block No. 177/1, Village -Ukharla, Tehsil Ghogha, ...

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A LIGNOSPAN FORTE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LIGNOSPAN FORTE, including repackagers and relabelers. The FDA regulates LIGNOSPAN FORTE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LIGNOSPAN FORTE 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 LIGNOSPAN FORTE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A LIGNOSPAN FORTE supplier is an individual or a company that provides LIGNOSPAN FORTE active pharmaceutical ingredient (API) or LIGNOSPAN FORTE finished formulations upon request. The LIGNOSPAN FORTE suppliers may include LIGNOSPAN FORTE API manufacturers, exporters, distributors and traders.
click here to find a list of LIGNOSPAN FORTE suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A LIGNOSPAN FORTE written confirmation (LIGNOSPAN FORTE WC) is an official document issued by a regulatory agency to a LIGNOSPAN FORTE manufacturer, verifying that the manufacturing facility of a LIGNOSPAN FORTE active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting LIGNOSPAN FORTE APIs or LIGNOSPAN FORTE finished pharmaceutical products to another nation, regulatory agencies frequently require a LIGNOSPAN FORTE WC (written confirmation) as part of the regulatory process.
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