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. ZCL Chemicals Limited
03 1M/s Dr. Reddy's Laboratories
04 1M/s Dr. Reddy's Laboratories Ltd
05 1M/s Dr. Reddy's Laboratories
06 1M/s BDR Lifesciences Pvt Ltd
07 1M/s Honour labs Ltd
08 1M/s MSN Laboratories
09 1M/s MSN Organics Pvt Ltd
10 1M/s Sharon Bio-Medicine
11 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
12 1M/s. Cadila Pharmaceuticals Ltd.,
13 1M/s. Hetro Labs Limited
14 1M/s. Mylan Laboratories Ltd.,
15 1M/s. Sun Pharmaceuticals Ltd.
16 1M/s. Unichem Lab. Ltd.
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01 1ATOMOXETIN HCL EP/USP
02 1Atomoxetine BP/IP/USP
03 1Atomoxetine Hydrochloride
04 1Atomoxetine Hydrochloride (IH
05 1Atomoxetine Hydrochloride (IH)
06 1Atomoxetine Hydrochloride (IH/EP/USP)
07 1Atomoxetine Hydrochloride (Ph. Eur./IH)
08 1Atomoxetine Hydrochloride EP/USP
09 3Atomoxetine Hydrochloride IH
10 3Atomoxetine Hydrochloride USP
11 1Atomoxetine Hydrochloride USP/EP
12 1Lilly brand of atomoxetine hydrochloride EP/USP
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01 1TFDA-0002291
02 1WC-0023
03 1WC-0035A3
04 1WC-0035a
05 1WC-0041
06 1WC-0062
07 1WC-0074Amended
08 1WC-0118
09 1WC-0153
10 1WC-0168
11 1WC-0195
12 1WC-0281A3
13 1WC-0281new2
14 1WC-0340
15 1WC-0362
16 1WC-0390
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01 15India
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 : 2025-07-15
Written Confirmation Number : TFDA-0002291
Address of the Firm : No. 168, Kai Yuan Rd, Hsin-Ying, Tainan City 73055, Taiwan
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
Atomoxetine Hydrochloride EP/USP
Date of Issue : 2022-08-25
Valid Till : 2025-07-02
Written Confirmation Number : WC-0195
Address of the Firm : Plot No. 3102/B, GIDC, Industrial Estate, Ankleshwar-393 002, Bharuch, Gujarat I...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-07-28
Valid Till : 2025-11-30
Written Confirmation Number : WC-0390
Address of the Firm : CTO-SEZ-Process Unit-01, Sector No 28 to 34, 36 to 37, 40, 50 to 53 & 03, Survey...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-15
Valid Till : 2025-06-25
Written Confirmation Number : WC-0035A3
Address of the Firm : Chemical Technical Operations Unit-V, Plot No 116, Sri Venkateshwara, Jinnaram M...
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-06
Valid Till : 2025-06-25
Written Confirmation Number : WC-0035a
Address of the Firm : Chemical Technical Operations Unit-V, Plot No 116, Sri Venkateshwara, Jinnaram M...
Atomoxetine Hydrochloride (IH/EP/USP)
Date of Issue : 2022-09-01
Valid Till : 2025-07-02
Written Confirmation Number : WC-0074Amended
Address of the Firm : 294, GIDC Estate, Ankleshwar-393 002, Bharuch, Gujarat, India
Atomoxetine Hydrochloride (IH)
Date of Issue : 2022-09-16
Valid Till : 2025-08-08
Written Confirmation Number : WC-0041
Address of the Firm : Unit-I, Survey No.10, I.D.A, Gaddapotharam Village, Jinnaram Mandal,Medak Dist, ...
Date of Issue : 2022-08-11
Valid Till : 2025-07-02
Written Confirmation Number : WC-0153
Address of the Firm : Plot No. L-6, MIDC Taloja,Tal.Panvel, District-Raigad-41 0208,\r\nMaharashtra, I...
Atomoxetine Hydrochloride USP/EP
Date of Issue : 2022-08-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0168
Address of the Firm : Plot No. 24/2, & 25, Phase -IV, GIDC, Industrial Zone, At & Post - Panoli, Dist....
Date of Issue : 2022-06-17
Valid Till : 2025-07-21
Written Confirmation Number : WC-0062
Address of the Firm : Plot No.197, Sector 1, Pithampur, Dist. Dhar, M.P
78
PharmaCompass offers a list of Atomoxetin Hydrochloride 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 Atomoxetin Hydrochloride manufacturer or Atomoxetin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Atomoxetin Hydrochloride manufacturer or Atomoxetin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Atomoxetin Hydrochloride API Price utilized in the formulation of products. Atomoxetin Hydrochloride API Price is not always fixed or binding as the Atomoxetin Hydrochloride Price is obtained through a variety of data sources. The Atomoxetin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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, COA and API Price 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, COA and API Price related information on PharmaCompass.
A Strattera (TN) written confirmation (Strattera (TN) WC) is an official document issued by a regulatory agency to a Strattera (TN) manufacturer, verifying that the manufacturing facility of a Strattera (TN) active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Strattera (TN) APIs or Strattera (TN) finished pharmaceutical products to another nation, regulatory agencies frequently require a Strattera (TN) WC (written confirmation) as part of the regulatory process.
click here to find a list of Strattera (TN) suppliers with Written Confirmation (WC) on PharmaCompass.
We have 13 companies offering Strattera (TN)
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