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 1Bhavna Laboratories
03 1Jai Radhe Sales
04 1Rampex Labs
05 1Biophore India Pharmaceuticals Pvt Ltd
06 1Transo-Pharm Handels GmbH
07 1HRV Pharma
08 1Tenatra Exports
09 1Atomgrid
10 1Auro Laboratories
11 1Biotechnica DWC
12 1Celanese
13 1Centaur Pharmaceuticals
14 1Chemvisai Labs
15 1Cilag AG
16 1Daiwa Pharmaceuticals
17 1Dasami Lab
18 1Erythro Pharma
19 1Everest Organics
20 1Guangzhou Tosun Pharmaceutical
21 1Helsinn Advanced Synthesis
22 1Hoventa Pharma
23 1Indoco Remedies Limited
24 1LifeFirst Pharma
25 1Mallinckrodt Pharmaceuticals
26 1Meck Pharma
27 1Medinex Laboratories
28 1Procos
29 1Saurav Chemicals
30 1Seven Star Pharmaceutical
31 1Shreepati Pharmaceuticals
32 1Sionc Pharmaceuticals
33 1Sneha Medicare Pvt Ltd
34 1Syn-Tech Chem. & Pharm
35 1Tecoland Corporation
36 1Tokuyama Corporation
37 1Vivachem Intermediates
38 5Blank
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01 1Algeria
02 1China
03 1Germany
04 25India
05 1Ireland
06 1Italy
07 1Japan
08 2Switzerland
09 2Taiwan
10 2U.S.A
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01 7Active
02 10Inactive
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01 1TFDA-0002291
02 1WC-0085n
03 1WC-0171
04 1WC-0273
05 1WC-0416
06 1WC-0578
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01 120230720-211-J-1521
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01 143235-0005
02 146016-9522
03 154871-0001
04 158159-030
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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 : 2016-12-01
Pay. Date : 2016-09-15
DMF Number : 30862
Submission : 2016-09-12
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 : 58159-030
Start Marketing Date : 2024-12-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2023-07-20
Registration Number : 20230720-211-J-1521
Manufacturer Name : Nuray Chemicals Private Limited
Manufacturer Address : No.111, SIDCO Industrial Estate, Kakkalur, Thiruvallur District, Tamil Nadu-602 003, India
Bhavna Laboratories is an API & Intermediate manufacturer focusing on the muscle relaxant & ophthalmic segments.
Rampex Labs – Simplifying Synthesis with Innovation, Quality, and Commitment to Global Pharmaceutical Excellence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35300
Submission : 2020-10-31
Status : Active
Type : II
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-03-23
Pay. Date : 2020-02-12
DMF Number : 32843
Submission : 2018-06-26
Status : Active
Type : II
Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Date of Issue : 2022-02-22
Valid Till : 2025-07-15
Written Confirmation Number : TFDA-0002291
Address of the Firm :
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33920
Submission : 2019-06-06
Status : Active
Type : II
Date of Issue : 2025-09-16
Valid Till : 2028-08-13
Written Confirmation Number : WC-0171
Address of the Firm :
NDC Package Code : 43235-0005
Start Marketing Date : 2016-08-17
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 : 4797
Submission : 1983-01-31
Status : Inactive
Type : II

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PharmaCompass offers a list of Chlorzoxazone 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 Chlorzoxazone manufacturer or Chlorzoxazone supplier for your needs.
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A Neoflex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Neoflex, including repackagers and relabelers. The FDA regulates Neoflex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Neoflex 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 Neoflex supplier is an individual or a company that provides Neoflex active pharmaceutical ingredient (API) or Neoflex finished formulations upon request. The Neoflex suppliers may include Neoflex API manufacturers, exporters, distributors and traders.
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We have 37 companies offering Neoflex
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