TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1TAPI Technology & API Services
02 1Abbott Laboratories
03 1Alembic Pharmaceuticals Limited
04 2Biocon
05 3Chongqing DaXin Pharmaceutical
06 1Concord Biotech
07 2Ercros
08 1Krebs Biochemicals & Industries Ltd
09 2Lek Pharmaceuticals
10 1Livzon New North River Pharmaceutical
11 3Lupin Ltd
12 1Merck & Co
13 2RANBAXY LABORATORIES LIMITED
14 2Recordati
15 1Sterling Biotech
16 1Syngen Biotech
17 1Yung Shin Pharmaceutical Industrial
18 1Zhejiang Apeloa Kangyu Pharmaceutical Co. Ltd
19 1Zhejiang Hisun Pharmaceutical
20 2Zhejiang Ruibang Laboratories
TAPI offers customized CDMO Solutions for API development and manufacturing services.
GDUFA
DMF Review : Complete
Rev. Date : 2012-12-27
Pay. Date : 2012-12-03
DMF Number : 11502
Submission : 1995-05-12
Status :
Type : II
A Lovastatin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lovastatin, including repackagers and relabelers. The FDA regulates Lovastatin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lovastatin 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 Lovastatin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lovastatin supplier is an individual or a company that provides Lovastatin active pharmaceutical ingredient (API) or Lovastatin finished formulations upon request. The Lovastatin suppliers may include Lovastatin API manufacturers, exporters, distributors and traders.
click here to find a list of Lovastatin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Lovastatin DMF (Drug Master File) is a document detailing the whole manufacturing process of Lovastatin active pharmaceutical ingredient (API) in detail. Different forms of Lovastatin DMFs exist exist since differing nations have different regulations, such as Lovastatin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lovastatin DMF submitted to regulatory agencies in the US is known as a USDMF. Lovastatin USDMF includes data on Lovastatin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lovastatin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lovastatin suppliers with USDMF on PharmaCompass.
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