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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01 1Nuray Chemicals Private Limited
02 1Bal Pharma
03 1Synthokem Labs
04 1LGM Pharma
05 1Temad Co
06 1HRV Global Life Sciences
07 1Atman Pharma Private Limited
08 1Granules India Limited
09 1Abbott Laboratories
10 1Ajinomoto Company
11 1Almelo
12 1Aurore Life Sciences
13 1Bioindustria L.I.M. Spa
14 1EURAND
15 1Heumann
16 1MSN Laboratories
17 1SKVen Technologies Pvt. Ltd
18 1Standard Chem. & Pharm. Co., Ltd
19 1Sumitomo Chemical
20 4Blank
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01 1China
02 1Germany
03 10India
04 1Iran
05 1Italy
06 2Japan
07 3U.S.A
08 4Blank
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01 7Active
02 9Inactive
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01 1Valid
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01 23Blank
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01 1WC-0119
02 1WC-0416
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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 : 2017-07-05
Pay. Date : 2017-05-12
DMF Number : 31628
Submission : 2017-06-16
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 : 58159-043
Start Marketing Date : 2020-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39220
Submission : 2024-01-03
Status : Active
Type : II
NDC Package Code : 58343-0140
Start Marketing Date : 2022-10-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-11-12
Pay. Date : 2020-09-29
DMF Number : 35210
Submission : 2020-09-30
Status : Active
Type : II
NDC Package Code : 62207-974
Start Marketing Date : 2021-04-06
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 : 7032
Submission : 1987-06-17
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6183
Submission : 1986-02-06
Status : Inactive
Type : II
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PharmaCompass offers a list of Prazosin 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 Prazosin Hydrochloride manufacturer or Prazosin Hydrochloride supplier for your needs.
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A Vasoflex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vasoflex, including repackagers and relabelers. The FDA regulates Vasoflex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vasoflex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Vasoflex supplier is an individual or a company that provides Vasoflex active pharmaceutical ingredient (API) or Vasoflex finished formulations upon request. The Vasoflex suppliers may include Vasoflex API manufacturers, exporters, distributors and traders.
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We have 19 companies offering Vasoflex
Get in contact with the supplier of your choice: