Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Cohance Lifesciences
02 1Dr. Reddy's Laboratories
03 1SCI Pharmtech
04 1Apotex Pharmachem
05 1Aurobindo Pharma Limited
06 1Cadila Pharmaceuticals
07 1Glenmark Life Sciences
08 1Hetero Drugs
09 1MSN Laboratories
10 1Macleods Pharmaceuticals Limited
11 1Olon S.p.A
12 1Sun Pharmaceutical Industries Limited
13 1Teva Pharmaceutical Industries
14 1Unichem Laboratories Limited
15 1Viatris
16 1Zhejiang Jiuzhou Pharmaceutical
17 1Zydus Lifesciences
01 1ATOMOXETINE HCL USP
02 5ATOMOXETINE HYDROCHLORIDE
03 1ATOMOXETINE HYDROCHLORIDE DRUG SUBSTANCE
04 9ATOMOXETINE HYDROCHLORIDE USP
05 1ATOMOXETINE HYDROCHLORIDE USP [ROUTE CODE "MY"]
01 1Canada
02 1China
03 11India
04 1Israel
05 1Italy
06 1Taiwan
07 1U.S.A
01 15Active
02 2Inactive
01 8Complete
02 9Blank
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2019-12-27
Pay. Date : 2019-12-03
DMF Number : 29211
Submission : 2015-03-26
Status : Active
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18440
Submission : 2005-06-22
Status : Active
Type : II
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
GDUFA
DMF Review : Complete
Rev. Date : 2020-12-12
Pay. Date : 2020-11-09
DMF Number : 32363
Submission : 2018-06-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20070
Submission : 2007-05-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19605
Submission : 2007-03-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20246
Submission : 2007-02-07
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20552
Submission : 2007-05-21
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2012-11-23
Pay. Date : 2012-11-13
DMF Number : 20499
Submission : 2007-04-30
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2023-09-07
Pay. Date : 2023-08-31
DMF Number : 19861
Submission : 2006-10-12
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20364
Submission : 2007-03-22
Status : Active
Type : II
A Atomoxetine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atomoxetine Hydrochloride, including repackagers and relabelers. The FDA regulates Atomoxetine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atomoxetine Hydrochloride 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 Atomoxetine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atomoxetine Hydrochloride supplier is an individual or a company that provides Atomoxetine Hydrochloride active pharmaceutical ingredient (API) or Atomoxetine Hydrochloride finished formulations upon request. The Atomoxetine Hydrochloride suppliers may include Atomoxetine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Atomoxetine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Atomoxetine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Atomoxetine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Atomoxetine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Atomoxetine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Atomoxetine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Atomoxetine Hydrochloride USDMF includes data on Atomoxetine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Atomoxetine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Atomoxetine Hydrochloride suppliers with USDMF on PharmaCompass.
We have 17 companies offering Atomoxetine Hydrochloride
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