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 1LGM Pharma
03 1HRV Pharma
04 1Willow Birch Pharma
05 1Alchymars ICM SM
06 2Alivus Life Sciences
07 1Aurobindo Pharma Limited
08 1Chromo Laboratories
09 1Dishman Carbogen Amcis
10 1Divis Laboratories
11 1Glenmark Pharmaceuticals
12 1Globofarm International
13 2Hetero Drugs
14 1Ipca Laboratories
15 1Matrix Pharmaceutical Inc
16 1NGL Fine-Chem
17 1Qingdao Qingmei Biotech
18 1Rolabo Outsourcing
19 1Shanghai Desano Bio-Pharmaceutical
20 1Shanghai Desano Chemical Pharmaceutical Co., Ltd.
21 1Taro Pharmaceutical Industries
22 1USV Private Limited
23 1Unipex
24 1Viatris
25 1Zydus Lifesciences
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01 3China
02 1France
03 17India
04 1Spain
05 5U.S.A
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01 12Active
02 3Inactive
03 12Blank
01 7Valid
02 20Blank
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01 1307MF10070
02 1307MF10098
03 25Blank
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01 2WC-0040
02 1WC-0057n
03 1WC-0091
04 1WC-0416
05 22Blank
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01 27Blank
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01 114998-0006
02 157451-1227
03 159651-090
04 162147-0057
05 162331-059
06 165841-158
07 165977-0034
08 165977-0159
09 166039-928
10 184206-0014
11 17Blank
01 27Blank
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 36339
Submission : 2021-10-11
Status : Active
Type : II
Date of Issue : 2024-02-20
Valid Till : 2026-12-06
Written Confirmation Number : WC-0416
Address of the Firm :
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Willow Birch Pharma delivers trusted, high-quality APIs nationwide with unmatched service, compliance, and competitive value.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-23
Pay. Date : 2014-05-16
DMF Number : 22121
Submission : 2008-10-27
Status : Active
Type : II
Certificate Number : CEP 2015-346 - Rev 02
Issue Date : 2025-04-03
Type : Chemical
Substance Number : 2192
Status : Valid
Registration Number : 307MF10098
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Maharashtra, India
Initial Date of Registration : 2025-08-06
Latest Date of Registration :
Date of Issue : 2022-07-06
Valid Till : 2025-06-25
Written Confirmation Number : WC-0057n
Address of the Firm :
NDC Package Code : 66039-928
Start Marketing Date : 2016-12-30
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : Reviewed
Rev. Date : 2017-03-02
Pay. Date : 2017-01-05
DMF Number : 31142
Submission : 2016-12-30
Status : Active
Type : II
Certificate Number : CEP 2018-150 - Rev 04
Issue Date : 2025-04-03
Type : Chemical
Substance Number : 2192
Status : Valid

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 43622
Submission : 2026-02-12
Status : Active
Type : II

✕ Product Not Available For Sales
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-09-15
Pay. Date : 2013-03-22
DMF Number : 26906
Submission : 2013-03-21
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22057
Submission : 2008-10-01
Status : Active
Type : II
NDC Package Code : 14998-0006
Start Marketing Date : 2005-10-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25305
Submission : 2011-09-13
Status : Inactive
Type : II

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PharmaCompass offers a list of Atovaquone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Atovaquone manufacturer or Atovaquone supplier for your needs.
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A Wellvone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Wellvone, including repackagers and relabelers. The FDA regulates Wellvone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Wellvone 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 Wellvone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Wellvone supplier is an individual or a company that provides Wellvone active pharmaceutical ingredient (API) or Wellvone finished formulations upon request. The Wellvone suppliers may include Wellvone API manufacturers, exporters, distributors and traders.
click here to find a list of Wellvone suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
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