Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.

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01 1Malladi Drugs & Pharmaceuticals Limited
02 1Supriya Lifescience Ltd
03 7Supriya Lifescience Ltd.
04 2Auro Laboratories Limited
05 2Keshava Organics Pvt. Ltd.
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01 1Ace Biopharm Co., Ltd.
02 2Daeshin Muyak Co., Ltd.
03 1Farmist Co., Ltd.
04 1G-Max Pharmachem Co., Ltd.
05 1Gukjeon Co., Ltd.
06 1IMCD Korea Co., Ltd.
07 1Narsha Farm Co., Ltd.
08 1Pharmaline Co., Ltd.
09 1Pharmapia Co., Ltd.
10 1Sam-O Pharmaceutical Co., Ltd.
11 1Sanil Pharma Co., Ltd.
12 1Sungjin Exim Co., Ltd.
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01 13Chlorpheniramine maleate
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01 13India
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Registrant Name : Ace Biopharm Co., Ltd.
Registration Date : 2026-04-14
Registration Number : 20260414-210-J-2179
Manufacturer Name : Malladi Drugs & Pharmaceutic...
Manufacturer Address : Unit-5, Plot No: 49, 50, 55 & 56, IDA, Gajulamandyam, Attur (PO), Rnigunta-517 520, T...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Sungjin Exim Co., Ltd.
Registration Date : 2026-04-28
Registration Number : 20201217-210-J-552(A)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed, Dist- Ratnagiri 415722, Maharas...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : G-Max Pharmachem Co., Ltd.
Registration Date : 2024-11-18
Registration Number : 20201217-210-J-552(6)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC, Tal.-Khed, Dist.-Ratnagiri, pin: 415 722...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : IMCD Korea Co., Ltd.
Registration Date : 2021-04-12
Registration Number : 20201217-210-J-552(1)
Manufacturer Name : Supriya Lifescience Ltd
Manufacturer Address : A-5/2, Lote-Parshuram Industrial Area, MIDC, Taluka-Khed, Dist.-Ratnagiri, 415722, Ma...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Sam-O Pharmaceutical Co., Ltd.
Registration Date : 2020-12-17
Registration Number : 20201217-210-J-552
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed, Dist- Ratnagiri 415722, Maharas...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Narsha Farm Co., Ltd.
Registration Date : 2024-09-05
Registration Number : 20201217-210-J-552(5)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed, Dist- Ratnagiri 415722, Maharas...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Daeshin Muyak Co., Ltd.
Registration Date : 2021-12-08
Registration Number : 20201217-210-J-552(2)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram IndustrialArea, MIDC, Tal-Khed, Dist-Ratnagiri, 415722 Maharash...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Gukjeon Co., Ltd.
Registration Date : 2022-04-27
Registration Number : 20201217-210-J-552(3)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC, Tal-Khed, Dist-Ratnagiri, 415722, Mahara...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Registrant Name : Sanil Pharma Co., Ltd.
Registration Date : 2023-06-30
Registration Number : 20201217-210-J-552(4)
Manufacturer Name : Supriya Lifescience Ltd.
Manufacturer Address : A-5/2, Lote Parshuram Industrial Area, MIDC Tal-Khed, Dist- Ratnagiri 415722, Maharas...
Registrant Name : Daeshin Muyak Co., Ltd.
Registration Date : 2026-04-01
Registration Number : 20260330-210-J-2140(A)
Manufacturer Name : Auro Laboratories Limited
Manufacturer Address : K-56, MIDC, Tarapur, Thane 401506, Maharashtra State, India

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PharmaCompass offers a list of Chlorpheniramine Maleate 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 Chlorpheniramine Maleate manufacturer or Chlorpheniramine Maleate supplier for your needs.
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A Alunex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alunex, including repackagers and relabelers. The FDA regulates Alunex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alunex 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 Alunex manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Alunex supplier is an individual or a company that provides Alunex active pharmaceutical ingredient (API) or Alunex finished formulations upon request. The Alunex suppliers may include Alunex API manufacturers, exporters, distributors and traders.
click here to find a list of Alunex suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Alunex Drug Master File in Korea (Alunex KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Alunex. The MFDS reviews the Alunex KDMF as part of the drug registration process and uses the information provided in the Alunex KDMF to evaluate the safety and efficacy of the drug.
After submitting a Alunex KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Alunex API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Alunex suppliers with KDMF on PharmaCompass.
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