Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience
02 2Neuland Laboratories
03 1Amphastar Pharmaceuticals
04 1AstraZeneca
05 1Boehringer Ingelheim GmbH
06 2Cambrex Corporation
07 3Cipla
08 1FDC
09 2GSK
10 2Huhtamaki
11 1Laboratorio Chimico Internazionale Spa
12 1Lupin Ltd
13 1Lusochimica
14 1Melody Healthcare Pvt Ltd
15 1Olon S.p.A
16 1RP SCHERER GMBH & CO. KG
17 1Teva Pharmaceutical Industries
18 4Blank
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 30708
Submission : 2016-06-27
Status :
Type : II
Neuland Laboratories- A dedicated 100% API provider.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16104
Submission : 2002-08-16
Status :
Type : II
Neuland Laboratories- A dedicated 100% API provider.
GDUFA
DMF Review : Complete
Rev. Date : 2013-09-26
Pay. Date : 2013-08-29
DMF Number : 16371
Submission : 2003-01-20
Status :
Type : II
A Fartolin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fartolin, including repackagers and relabelers. The FDA regulates Fartolin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fartolin 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 Fartolin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fartolin supplier is an individual or a company that provides Fartolin active pharmaceutical ingredient (API) or Fartolin finished formulations upon request. The Fartolin suppliers may include Fartolin API manufacturers, exporters, distributors and traders.
click here to find a list of Fartolin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Fartolin DMF (Drug Master File) is a document detailing the whole manufacturing process of Fartolin active pharmaceutical ingredient (API) in detail. Different forms of Fartolin DMFs exist exist since differing nations have different regulations, such as Fartolin USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Fartolin DMF submitted to regulatory agencies in the US is known as a USDMF. Fartolin USDMF includes data on Fartolin's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fartolin USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Fartolin suppliers with USDMF on PharmaCompass.
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