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 13M Company
04 3AMINO GmbH
05 1Hengdian Group
06 1Jinan Pengbo Biotechnology
07 1PharmHe Global Corp
08 1SIGMA TAU
01 3China
02 3Germany
03 2India
04 2U.S.A
01 4Active
02 2Inactive
03 4Blank
01 10Blank
01 1225MF10183
02 9Blank
01 1WC-0416
02 9Blank
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 : 2020-04-24
Pay. Date : 2020-03-10
DMF Number : 34404
Submission : 2020-03-12
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 : 58159-076
Start Marketing Date : 2019-11-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
HRV Global Life Sciences - Market Expansion Leader in Pharmaceuticals.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11079
Submission : 1994-09-08
Status : Active
Type : II
NDC Package Code : 46052-0196
Start Marketing Date : 1997-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-03-01
Pay. Date : 2017-10-27
DMF Number : 31655
Submission : 2017-03-28
Status : Active
Type : II
NDC Package Code : 46052-0196
Start Marketing Date : 1997-01-01
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 : 15348
Submission : 2001-03-23
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5082
Submission : 1983-09-30
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11069
Submission : 1994-09-08
Status : Inactive
Type : II
Registration Number : 225MF10183
Registrant's Address : An der Zucker-Raffinerie 9, 38373 Frellstedt, Germany
Initial Date of Registration : 2013-09-25
Latest Date of Registration : --
NDC Package Code : 46052-0196
Start Marketing Date : 1997-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Betaine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Betaine, including repackagers and relabelers. The FDA regulates Betaine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Betaine 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 Betaine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Betaine supplier is an individual or a company that provides Betaine active pharmaceutical ingredient (API) or Betaine finished formulations upon request. The Betaine suppliers may include Betaine API manufacturers, exporters, distributors and traders.
click here to find a list of Betaine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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