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 1AASraw Biochemical Technology Co., Ltd
04 1ASG Biochem
05 2Curia
06 1Gedeon Richter
07 1Hikma Pharmaceuticals
08 1Merck & Co
09 1Olon S.p.A
10 1ScinoPharm Taiwan, Ltd
11 1Shouyuan Chemical
12 1Swati Spentose
13 1Trifarma
01 2China
02 1Hungary
03 4India
04 2Italy
05 1Taiwan
06 3U.S.A
07 1United Kingdom
01 5Active
02 4Inactive
03 5Blank
01 14Blank
01 14Blank
01 1WC-0416
02 13Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-12-05
Pay. Date : 2017-07-28
DMF Number : 31920
Submission : 2017-10-28
Status : Active
Type : II
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm :
NDC Package Code : 58159-046
Start Marketing Date : 2024-08-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20344
Submission : 2007-03-06
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16598
Submission : 2003-05-22
Status : Active
Type : II
NDC Package Code : 55486-1570
Start Marketing Date : 2012-06-03
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 : 34723
Submission : 2020-03-17
Status : Active
Type : II
NDC Package Code : 55486-1570
Start Marketing Date : 2012-06-03
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 : 17962
Submission : 2005-01-05
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15427
Submission : 2001-05-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17459
Submission : 2004-06-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16217
Submission : 2002-10-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16938
Submission : 2003-10-31
Status : Inactive
Type : II
NDC Package Code : 65129-1066
Start Marketing Date : 2001-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Oxandrolone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxandrolone, including repackagers and relabelers. The FDA regulates Oxandrolone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxandrolone 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 Oxandrolone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxandrolone supplier is an individual or a company that provides Oxandrolone active pharmaceutical ingredient (API) or Oxandrolone finished formulations upon request. The Oxandrolone suppliers may include Oxandrolone API manufacturers, exporters, distributors and traders.
click here to find a list of Oxandrolone suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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