Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
01 1M/s Centrient Pharmaceuticals India Private Limited
02 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
03 1 M/s. Aurobindo Pharma Ltd.
01 1Dicloxacillin Sodium (BP/Ph. Eur)
02 1Dicloxacillin Sodium (Ph. Eur)
03 1Dicloxacillin Sodium IP/BP/USP/EP
01 1WC-0010
02 1WC-0023
03 1WC-0121
01 3India
Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.
Dicloxacillin Sodium IP/BP/USP/EP
Date of Issue : 2022-05-19
Valid Till : 2025-05-27
Written Confirmation Number : WC-0010
Address of the Firm : Bhai Mohan Singh Nagar, Toansa, District SBS Nagar,(Nawanshahr), Punjab - 144 53...
Dicloxacillin Sodium (BP/Ph. Eur)
Date of Issue : 2019-07-05
Valid Till : 2022-07-02
Written Confirmation Number : WC-0121
Address of the Firm : Unit-V, Plot No.79-91, IDA, Chemical Zone, Pashamylaram (V), Patancheru (M), Med...
Dicloxacillin Sodium (Ph. Eur)
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Sy.No.1/22, 2/1 To 5, 6 to 18, 61 to 69, Pydibhimavaram Village, Ranasthalam, Sr...
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A Diflor manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diflor, including repackagers and relabelers. The FDA regulates Diflor manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diflor 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 Diflor supplier is an individual or a company that provides Diflor active pharmaceutical ingredient (API) or Diflor finished formulations upon request. The Diflor suppliers may include Diflor API manufacturers, exporters, distributors and traders.
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A Diflor written confirmation (Diflor WC) is an official document issued by a regulatory agency to a Diflor manufacturer, verifying that the manufacturing facility of a Diflor active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Diflor APIs or Diflor finished pharmaceutical products to another nation, regulatory agencies frequently require a Diflor WC (written confirmation) as part of the regulatory process.
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