01 1Novartis Pharmaceuticals Corporation
02 1Sun Pharmaceutical Industries Limited
01 1India
02 1Switzerland
01 2Active
01 2Blank
01 1227MF10097
02 1Blank
01 2Blank
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GDUFA
DMF Review : Reviewed
Rev. Date : 2018-12-03
Pay. Date : 2018-11-19
DMF Number : 32895
Submission : 2018-11-06
Status : Active
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9906
Submission : 1992-10-09
Status : Active
Type : II
Registration Number : 227MF10097
Registrant's Address : Lichtstrasse 35, CH-4056 Basel, Switzerland
Initial Date of Registration : 2015-04-09
Latest Date of Registration : --
A Pentetreotide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pentetreotide, including repackagers and relabelers. The FDA regulates Pentetreotide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pentetreotide API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Pentetreotide supplier is an individual or a company that provides Pentetreotide active pharmaceutical ingredient (API) or Pentetreotide finished formulations upon request. The Pentetreotide suppliers may include Pentetreotide API manufacturers, exporters, distributors and traders.
click here to find a list of Pentetreotide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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