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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Chlorpheniramine Maleate manufacturer or Chlorpheniramine Maleate supplier.
A Alka-seltzer plus manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Alka-seltzer plus, including repackagers and relabelers. The FDA regulates Alka-seltzer plus manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Alka-seltzer plus 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 Alka-seltzer plus manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Alka-seltzer plus supplier is an individual or a company that provides Alka-seltzer plus active pharmaceutical ingredient (API) or Alka-seltzer plus finished formulations upon request. The Alka-seltzer plus suppliers may include Alka-seltzer plus API manufacturers, exporters, distributors and traders.
click here to find a list of Alka-seltzer plus 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 Alka-seltzer plus Drug Master File in Korea (Alka-seltzer plus KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Alka-seltzer plus. The MFDS reviews the Alka-seltzer plus KDMF as part of the drug registration process and uses the information provided in the Alka-seltzer plus KDMF to evaluate the safety and efficacy of the drug.
After submitting a Alka-seltzer plus 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 Alka-seltzer plus API can apply through the Korea Drug Master File (KDMF).
click here to find a list of Alka-seltzer plus suppliers with KDMF on PharmaCompass.
We have 4 companies offering Alka-seltzer plus
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