Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1CENTRIENT PHARMACEUTICALS INDIA PRIVATE LIMITED
02 3Dr. Reddy's Laboratories Ltd.
03 1Aurobindo Pharma Limited
04 1Biocon Limited
05 1Hetero Labs Limited
06 1JUBILANT PHARMOVA LIMITED
07 2Kyongbo Pharmaceutical Co. , Ltd.
08 1Morepen Laboratories Limited
09 1Novartis Pharmaceutical Manufacturing LLC
10 1Pharmacostech CO. ,LTD
11 1ST Pharm Co. , Ltd.
12 2Synthimed Labs Private Limited
13 1YUIL PHARM TECH. C.O. , LTD.
14 1Yoshindo Co., Ltd.
15 1Zhejiang Hongyuan Pharmaceutical Co. , Ltd.
16 1Zhejiang Lepu Pharmaceutical Co. , Ltd.
01 1ATORVA STATN CALCIUM HYDRATE
02 1ATORVASTATIN CALCIUM TRIHYDRATE FORM-1
03 4Atorvastatin Calcium Hydrate
04 1Atorvastatin Calcium Hydrate (KBP)
05 1Atorvastatin Calcium Hydrate (for production only)
06 1Atorvastatin calcium
07 5Atorvastatin calcium hydrate
08 1Atorvastatin calcium hydrate (production only)
09 1Atorvastatin calcium hydrate [Form-I]
10 3Japanese Pharmacopoeia atorvastatin calcium hydrate
11 1atorvastatin calcium hydrate
01 2China
02 10India
03 2Japan
04 1Netherlands
05 1Slovenia
06 4South Korea
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Registration Number : 305MF10022
Registrant's Address : Bhai Mohan Singh Nagar, Toansa, District SBS Nagar (Nawanshahr), Punjab-144 533, Indi...
Initial Date of Registration : 2023-02-08
Latest Date of Registration : 2024-06-27
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 304MF10140
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2022-10-05
Latest Date of Registration : 2022-10-05
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
ATORVASTATIN CALCIUM TRIHYDRATE FORM-1
Registration Number : 226MF10020
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2014-01-21
Latest Date of Registration : 2014-01-21
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 228MF10199
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2016-10-19
Latest Date of Registration : 2016-10-19
Registration Number : 229MF10178
Registrant's Address : 20th KM Hosur Road, Electronics City, Bengaluru-560 100, Karnataka, India.
Initial Date of Registration : 2017-09-15
Latest Date of Registration : 2023-08-02
Registration Number : 304MF10117
Registrant's Address : Village-Bhagwanpur, Barwala Road, Derabassi-140 507 District-S. A. S. Nagar (Mohali)P...
Initial Date of Registration : 2022-08-10
Latest Date of Registration : 2022-08-10
Atorvastatin calcium hydrate (KBP)
Registration Number : 304MF10015
Registrant's Address : 174, Sirok-ro, Asan-si, Chungcheongnam-do, KOREA
Initial Date of Registration : 2022-01-20
Latest Date of Registration : 2022-01-20
Registration Number : 222MF10232
Registrant's Address : Verovskova ulica 57, 1000 Ljubljana, Slovenia
Initial Date of Registration : 2010-09-24
Latest Date of Registration : 2019-11-15
Registration Number : 302MF10070
Registrant's Address : 4th Floor, 416-418, Antriksh Bhawan, 22, Kasturba Gandhi Marg, New Delhi-110 001, Ind...
Initial Date of Registration : 2020-06-23
Latest Date of Registration : 2020-06-23
Atorvastatin calcium hydrate (for manufacturing purposes only)
Registration Number : 302MF10136
Registrant's Address : 47, Jeyakdanji-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Republic of Korea
Initial Date of Registration : 2020-11-18
Latest Date of Registration : 2020-11-18
A Lipitor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lipitor, including repackagers and relabelers. The FDA regulates Lipitor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lipitor 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 Lipitor manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lipitor supplier is an individual or a company that provides Lipitor active pharmaceutical ingredient (API) or Lipitor finished formulations upon request. The Lipitor suppliers may include Lipitor API manufacturers, exporters, distributors and traders.
click here to find a list of Lipitor suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Lipitor Drug Master File in Japan (Lipitor JDMF) empowers Lipitor 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 Lipitor JDMF during the approval evaluation for pharmaceutical products. At the time of Lipitor 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 Lipitor suppliers with JDMF on PharmaCompass.
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