01 1Creative Actives Private Limited
01 1Pharmapia Co., Ltd.
01 1Sodium picosulfate hydrate
01 1Blank
Registrant Name : Pharmapia Co., Ltd.
Registration Date : 2025-08-26
Registration Number : 20250826-211-J-1997
Manufacturer Name : Creative Actives Private Lim...
Manufacturer Address : Plot No. 15B6, APSEZ De-Notified Area, Atchuthapuram, Krishnapalem (V), Rambili (M), ...
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A Laxoberal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Laxoberal, including repackagers and relabelers. The FDA regulates Laxoberal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Laxoberal 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 Laxoberal supplier is an individual or a company that provides Laxoberal active pharmaceutical ingredient (API) or Laxoberal finished formulations upon request. The Laxoberal suppliers may include Laxoberal 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 Laxoberal Drug Master File in Korea (Laxoberal KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Laxoberal. The MFDS reviews the Laxoberal KDMF as part of the drug registration process and uses the information provided in the Laxoberal KDMF to evaluate the safety and efficacy of the drug.
After submitting a Laxoberal 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 Laxoberal API can apply through the Korea Drug Master File (KDMF).
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