Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 3Malladi Drug & Pharmaceuticals Limited
02 3Siegfried PharmaChemikalien Minden GmbH
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Registrant Name : Samil Pharmaceutical Co., Ltd.
Registration Date : 2013-09-12
Registration Number : 20050831-41-C-46-03(3)
Manufacturer Name : Malladi Drug & Pharmaceutica...
Manufacturer Address : 7B&7C, SIPCOT Industrial Complex, Ranipet-632 403, Ranipet District, Tamil Nadu, Indi...
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Registrant Name : Korea Johnson & Johnson Sales Co., Ltd.
Registration Date : 2024-09-11
Registration Number : 20050831-41-C-46-03(4)
Manufacturer Name : Malladi Drug & Pharmaceutica...
Manufacturer Address : 7B&7C, SIPCOT Industrial Complex, Ranipet-632 403, Ranipet District, Tamil Nadu, Indi...
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
Registrant Name : Kukjeon Pharmaceutical Co., Ltd.
Registration Date : 2005-08-31
Registration Number : 20050831-41-C-46-03
Manufacturer Name : Malladi Drug & Pharmaceutica...
Manufacturer Address : 7B&7C, SIPCOT Industrial Complex, Ranipet-632 403, Ranipet District, Tamil Nadu, Indi...
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PharmaCompass offers a list of Pseudoephedrine 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 Pseudoephedrine Hydrochloride manufacturer or Pseudoephedrine Hydrochloride supplier for your needs.
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A Sine-Off Maximum Strength No Drowsiness Formula Caplets manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sine-Off Maximum Strength No Drowsiness Formula Caplets, including repackagers and relabelers. The FDA regulates Sine-Off Maximum Strength No Drowsiness Formula Caplets manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sine-Off Maximum Strength No Drowsiness Formula Caplets 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 Sine-Off Maximum Strength No Drowsiness Formula Caplets supplier is an individual or a company that provides Sine-Off Maximum Strength No Drowsiness Formula Caplets active pharmaceutical ingredient (API) or Sine-Off Maximum Strength No Drowsiness Formula Caplets finished formulations upon request. The Sine-Off Maximum Strength No Drowsiness Formula Caplets suppliers may include Sine-Off Maximum Strength No Drowsiness Formula Caplets API manufacturers, exporters, distributors and traders.
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In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.
Pharmaceutical companies submit a Sine-Off Maximum Strength No Drowsiness Formula Caplets Drug Master File in Korea (Sine-Off Maximum Strength No Drowsiness Formula Caplets KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Sine-Off Maximum Strength No Drowsiness Formula Caplets. The MFDS reviews the Sine-Off Maximum Strength No Drowsiness Formula Caplets KDMF as part of the drug registration process and uses the information provided in the Sine-Off Maximum Strength No Drowsiness Formula Caplets KDMF to evaluate the safety and efficacy of the drug.
After submitting a Sine-Off Maximum Strength No Drowsiness Formula Caplets 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 Sine-Off Maximum Strength No Drowsiness Formula Caplets API can apply through the Korea Drug Master File (KDMF).
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