Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
01 2Mankind Pharma
02 1Centrient Pharmaceuticals
03 6Dr. Reddy's Laboratories
04 1ALP Pharm
05 1Amoli Organics
06 1Apotex Pharmachem
07 2Arch Pharmalabs
08 1Asymchem Laboratories
09 1Aurobindo Pharma Limited
10 3Biocon
11 2Cadila Pharmaceuticals
12 1Changzhou Pharmaceutical Factory
13 1Chromo Laboratories
14 1EPHAR BIOLOGICAL AND CHEMICAL CO LTD
15 1HEC Pharm
16 2Hetero Drugs
17 1Ind Swift Laboratories Limited
18 1Jiangsu Alpha Pharmaceutical Co., Ltd.
19 1Jubilant Generics
20 1Laurus Labs
21 1Lek Pharmaceuticals
22 3Lupin Ltd
23 3MSN Laboratories
24 2Macleods Pharmaceuticals Limited
25 3Morepen Laboratories
26 1Par Pharmaceutical
27 1Pfizer Inc
28 1Raks Pharma
29 1Signa S.A. de C.V.
30 4Sun Pharmaceutical Industries Limited
31 1Teva Pharmaceutical Industries
32 1Torrent Pharmaceuticals Limited
33 1Viatris
34 1Vijayasri Organics Limited
35 1Zhejiang Haisen Pharmaceutical Co., Ltd.
36 1Zhejiang Hisun Pharmaceutical
37 1Zhejiang Jiangbei Pharmaceutical
38 3Zhejiang Neo-Dankong Pharm. Co.,Ltd.
39 4Zydus Lifesciences
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
GDUFA
DMF Review : Complete
Rev. Date : 2022-01-12
Pay. Date : 2021-11-29
DMF Number : 34844
Submission : 2020-06-05
Status :
Type : II
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
GDUFA
DMF Review : Complete
Rev. Date : 2016-05-31
Pay. Date : 2015-08-20
DMF Number : 29520
Submission : 2015-08-03
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-27
Pay. Date : 2013-02-05
DMF Number : 18468
Submission : 2005-06-29
Status :
Type : II
Delivering quality and niche Active Pharmaceutical Ingredients across the global from our USFDA-approved facility.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36365
Submission : 2021-09-30
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2020-02-20
Pay. Date : 2020-01-28
DMF Number : 34423
Submission : 2019-12-31
Status :
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 : 25902
Submission : 2012-03-23
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2013-10-07
Pay. Date : 2013-09-25
DMF Number : 23664
Submission : 2010-03-30
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-27
Pay. Date : 2013-02-06
DMF Number : 21125
Submission : 2007-12-14
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2014-01-27
Pay. Date : 2013-01-04
DMF Number : 19997
Submission : 2006-11-27
Status :
Type : II
12
PharmaCompass offers a list of Atorvastatin 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 Atorvastatin manufacturer or Atorvastatin supplier for your needs.
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A Atorvastatin Calcium Trihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atorvastatin Calcium Trihydrate, including repackagers and relabelers. The FDA regulates Atorvastatin Calcium Trihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atorvastatin Calcium Trihydrate 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 Atorvastatin Calcium Trihydrate supplier is an individual or a company that provides Atorvastatin Calcium Trihydrate active pharmaceutical ingredient (API) or Atorvastatin Calcium Trihydrate finished formulations upon request. The Atorvastatin Calcium Trihydrate suppliers may include Atorvastatin Calcium Trihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Atorvastatin Calcium Trihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Atorvastatin Calcium Trihydrate DMF (Drug Master File) is a document detailing the whole manufacturing process of Atorvastatin Calcium Trihydrate active pharmaceutical ingredient (API) in detail. Different forms of Atorvastatin Calcium Trihydrate DMFs exist exist since differing nations have different regulations, such as Atorvastatin Calcium Trihydrate USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Atorvastatin Calcium Trihydrate DMF submitted to regulatory agencies in the US is known as a USDMF. Atorvastatin Calcium Trihydrate USDMF includes data on Atorvastatin Calcium Trihydrate's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Atorvastatin Calcium Trihydrate USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Atorvastatin Calcium Trihydrate suppliers with USDMF on PharmaCompass.
We have 39 companies offering Atorvastatin Calcium Trihydrate
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