SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
01 1SCI Pharmtech, Inc.
02 1Cadila Healthcare Limited
03 1Hetero Labs Limited
04 1Matrix Pharmacorp Private Limited
05 1Sicor Societa (') Italiana Corticosteroidi S. r. l.
06 1Syn-Tech Chem. & Pharm. Co. , Ltd.
07 1Tateyama Chemical Co., Ltd.
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
Atomoxetine Hydrochloride (Non-recrystallized crude)
Registration Number : 307MF10066
Registrant's Address : No. 61, Ln. 309, Haihu N. Rd. , Luzhu Dist. , Taoyuan City 33856, Taiwan
Initial Date of Registration : 2025-06-04
Latest Date of Registration : 2025-06-04
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PharmaCompass offers a list of Atomoxetine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Atomoxetine manufacturer or Atomoxetine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atomoxetine manufacturer or Atomoxetine supplier.
A Strattera (TN) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Strattera (TN), including repackagers and relabelers. The FDA regulates Strattera (TN) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Strattera (TN) 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 Strattera (TN) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Strattera (TN) supplier is an individual or a company that provides Strattera (TN) active pharmaceutical ingredient (API) or Strattera (TN) finished formulations upon request. The Strattera (TN) suppliers may include Strattera (TN) API manufacturers, exporters, distributors and traders.
click here to find a list of Strattera (TN) suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Strattera (TN) Drug Master File in Japan (Strattera (TN) JDMF) empowers Strattera (TN) API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Strattera (TN) JDMF during the approval evaluation for pharmaceutical products. At the time of Strattera (TN) JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Strattera (TN) suppliers with JDMF on PharmaCompass.
We have 7 companies offering Strattera (TN)
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