Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
Reset all filters
01 1Nuray Chemicals Private Limited
02 2Aarti Pharmalabs
03 1Farmhispania
04 1Amino Chemicals
05 1Aurobindo Pharma Limited
06 1CHEMO
07 1Grace
08 1Guangzhou Tosun Pharmaceutical
09 2Lupin Ltd
10 1Quimica Sintetica
11 1Rolabo Outsourcing
12 1ScinoPharm Taiwan, Ltd
13 1Sun Pharmaceutical Industries Limited
14 1Unimark Remedies Limited
15 2Wisdom Pharmaceutical
16 1Zhejiang Huahai Pharmaceutical
17 1Zydus Lifesciences
18 1Zydus Pharmaceuticals
Reset all filters
01 4China
02 9India
03 1Malta
04 4Spain
05 1Taiwan
06 2U.S.A
Reset all filters
01 13Active
02 4Inactive
03 4Blank
01 1Suspended by Holder
02 8Valid
03 12Blank
Reset all filters
01 1217MF11297
02 1227MF10089
03 19Blank
Reset all filters
01 1WC-0011nA2
02 1WC-0017
03 1WC-0095
04 1WC-0099
05 1WC-0170
06 1WC-0202
07 1WC-0416
08 14Blank
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 : 2022-10-28
Pay. Date : 2022-02-11
DMF Number : 36768
Submission : 2022-02-07
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 : 58159-086
Start Marketing Date : 2021-06-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-01-26
Pay. Date : 2023-10-05
DMF Number : 20097
Submission : 2006-12-27
Status : Active
Type : II
Certificate Number : R1-CEP 2011-197 - Rev 00
Issue Date : 2018-05-16
Type : Chemical
Substance Number : 2388
Status : Valid
Date of Issue : 2023-01-06
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm :
NDC Package Code : 15308-0900
Start Marketing Date : 1992-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-03-20
Pay. Date : 2020-03-18
DMF Number : 15457
Submission : 2001-05-04
Status : Active
Type : II
Certificate Number : R1-CEP 2009-261 - Rev 00
Issue Date : 2016-01-26
Type : Chemical
Substance Number : 2388
Status : Valid
NDC Package Code : 17404-0016
Start Marketing Date : 2003-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : CN |
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22846
Submission : 2009-06-09
Status : Active
Type : II
Certificate Number : R0-CEP 2023-055 - Rev 00
Issue Date : 2023-07-07
Type : Chemical
Substance Number : 2388
Status : Valid
NDC Package Code : 15308-0900
Start Marketing Date : 1992-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-08-16
Pay. Date : 2022-06-15
DMF Number : 19013
Submission : 2005-11-28
Status : Active
Type : II
Certificate Number : CEP 2008-232 - Rev 03
Issue Date : 2023-11-16
Type : Chemical
Substance Number : 2388
Status : Valid
Date of Issue : 2022-06-06
Valid Till : 2025-06-10
Written Confirmation Number : WC-0017
Address of the Firm :
NDC Package Code : 65862-346
Start Marketing Date : 2023-12-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-02-06
Pay. Date : 2013-01-17
DMF Number : 19479
Submission : 2006-05-31
Status : Active
Type : II
Certificate Number : R1-CEP 2008-273 - Rev 00
Issue Date : 2015-04-15
Type : Chemical
Substance Number : 2388
Status : Suspended by Holder
Date of Issue : 2024-04-23
Valid Till : 2027-04-22
Written Confirmation Number : WC-0170
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19697
Submission : 2006-08-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19148
Submission : 2006-02-02
Status : Active
Type : II
Registration Number : 217MF11297
Registrant's Address : MRA050X, INDUSTRIAL ESTATE MARSA MRS 3000 Malta
Initial Date of Registration : 2005-12-22
Latest Date of Registration :
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-07-15
Pay. Date : 2021-02-08
DMF Number : 33744
Submission : 2019-03-29
Status : Active
Type : II
NDC Package Code : 13612-0002
Start Marketing Date : 2019-03-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-07
Pay. Date : 2013-02-25
DMF Number : 17792
Submission : 2004-10-27
Status : Active
Type : II
Certificate Number : R1-CEP 2010-276 - Rev 00
Issue Date : 2017-06-02
Type : Chemical
Substance Number : 2388
Status : Valid
NDC Package Code : 64220-145
Start Marketing Date : 2005-12-01
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 : 37049
Submission : 2022-05-31
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-10-13
Pay. Date : 2014-10-03
DMF Number : 14720
Submission : 2000-02-21
Status : Active
Type : II
NDC Package Code : 22568-1136
Start Marketing Date : 2021-06-01
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 : 16072
Submission : 2002-07-22
Status : Active
Type : II
Certificate Number : CEP 2009-356 - Rev 03
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2388
Status : Valid
NDC Package Code : 65129-2021
Start Marketing Date : 2002-12-30
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 : 16857
Submission : 2003-09-12
Status : Inactive
Type : II
Date of Issue : 2022-07-13
Valid Till : 2025-07-04
Written Confirmation Number : WC-0202
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25738
Submission : 2012-02-07
Status : Inactive
Type : II
Certificate Number : R1-CEP 2015-322 - Rev 00
Issue Date : 2023-01-11
Type : Chemical
Substance Number : 2388
Status : Valid
NDC Package Code : 13612-0002
Start Marketing Date : 2019-03-21
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 : 15647
Submission : 2001-09-28
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15776
Submission : 2001-12-21
Status : Inactive
Type : II
Certificate Number : R1-CEP 2009-220 - Rev 01
Issue Date : 2016-08-26
Type : Chemical
Substance Number : 2388
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-06-02
Written Confirmation Number : WC-0011nA2
Address of the Firm :
Date of Issue : 2022-11-11
Valid Till : 2025-07-07
Written Confirmation Number : WC-0095
Address of the Firm :
Registration Number : 227MF10089
Registrant's Address : Poligono Industrial Malpica C/J, No. :3-4 50016 Zaragoza, Spain
Initial Date of Registration : 2015-03-12
Latest Date of Registration :
88
PharmaCompass offers a list of Benazepril Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier.
PharmaCompass also assists you with knowing the Benazepril Hydrochloride API Price utilized in the formulation of products. Benazepril Hydrochloride API Price is not always fixed or binding as the Benazepril Hydrochloride Price is obtained through a variety of data sources. The Benazepril Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Benazepril Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benazepril Hydrochloride, including repackagers and relabelers. The FDA regulates Benazepril Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benazepril Hydrochloride 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 Benazepril Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Benazepril Hydrochloride supplier is an individual or a company that provides Benazepril Hydrochloride active pharmaceutical ingredient (API) or Benazepril Hydrochloride finished formulations upon request. The Benazepril Hydrochloride suppliers may include Benazepril Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Benazepril Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 18 companies offering Benazepril Hydrochloride
Get in contact with the supplier of your choice: