Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1Nuray Chemicals Private Limited
02 1HRV Global Life Sciences
03 1Centaur Pharmaceuticals
04 2GSK
05 1Lonza Group
06 1Optimus Pharma
07 2Trifarma
01 4India
02 2Italy
03 1Switzerland
04 2United Kingdom
01 2Active
02 4Inactive
03 3Blank
01 9Blank
01 9Blank
01 1WC-0107
02 8Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
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GDUFA
DMF Review : Reviewed
Rev. Date : 2014-06-18
Pay. Date : 2013-02-08
DMF Number : 26808
Submission : 2013-02-18
Status : Active
Type : II
NDC Package Code : 58159-082
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-05-17
Pay. Date : 2019-05-13
DMF Number : 16522
Submission : 2003-02-27
Status : Active
Type : II
NDC Package Code : 46204-0130
Start Marketing Date : 2017-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10317
Submission : 1993-06-25
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 716
Submission : 1963-11-04
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4680
Submission : 1982-10-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7132
Submission : 1987-09-04
Status : Inactive
Type : II
NDC Package Code : 46204-0130
Start Marketing Date : 2017-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Date of Issue : 2022-06-08
Valid Till : 2025-06-25
Written Confirmation Number : WC-0107
Address of the Firm :
A Tranylcypromine Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tranylcypromine Sulfate, including repackagers and relabelers. The FDA regulates Tranylcypromine Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tranylcypromine Sulfate 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 Tranylcypromine Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tranylcypromine Sulfate supplier is an individual or a company that provides Tranylcypromine Sulfate active pharmaceutical ingredient (API) or Tranylcypromine Sulfate finished formulations upon request. The Tranylcypromine Sulfate suppliers may include Tranylcypromine Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Tranylcypromine Sulfate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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