Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1Zhejiang Hengkang Pharmaceutical
02 2M/s Glenmark Life Sciences Limited
03 1M/s. CTX Life Sciences Pvt. Ltd.,
04 1M/s. Piramal Enterprises Limited
05 1Mis. NOSCH LABS PVT LIMITED
01 1Amiodarone HCl EP/USP/BP
02 1Amiodarone Hydrochloride
03 1Amiodarone Hydrochloride (IP/BP/Ph.Eur/USP)
04 1Amiodarone Hydrochloride (Ph. Eur.)
05 1Amiodarone Hydrochloride EP
06 1Amiodarone Hydrochloride USP/EP
01 1WC-0057n
02 1WC-0097
03 1WC-0123
04 1WC-0310
05 1WC-0384A3
06 1ZJ220038
01 1China
02 5India
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Date of Issue : 2022-11-11
Valid Till : 2024-12-15
Written Confirmation Number : ZJ220038
Address of the Firm : No.11 Chengen Road, Pubagang Town, Sanmen, Zhejiang, China 317108
Amiodarone Hydrochloride (IP/BP/Ph.Eur/USP)
Date of Issue : 2023-12-28
Valid Till : 2026-12-28
Written Confirmation Number : WC-0310
Address of the Firm : Plot No. Z-103/l, Dahej SEZ, Phase ll, Dahej, Dist-Bharuch, Gujarat
Date of Issue : 2022-06-07
Valid Till : 2025-06-25
Written Confirmation Number : WC-0057n
Address of the Firm : Plot No. 3109, GIDC, Industrial Estate, Ankleshwar-393 002, Bharuch, Gujarat
Date of Issue : 2022-06-24
Valid Till : 2025-07-02
Written Confirmation Number : WC-0097
Address of the Firm : Block No. 251/P, 252/P, 253 to 255, 256/P,258/P, 276/P, 277/P, 278/P, 279 To 282...
Amiodarone Hydrochloride USP/EP
Date of Issue : 2022-09-02
Valid Till : 2023-01-05
Written Confirmation Number : WC-0384A3
Address of the Firm : Unit -IV Sy. No. 332,333 & 335, Velimindeu V Chityal Nalgonda District Telangan ...
Amiodarone Hydrochloride (Ph. Eur.)
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0123
Address of the Firm : Sy. Nos. 7-70, 70/1 & 70/2, Digwal Village, Kohir Mandai, Sangareddy District, T...
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A Ritmocardyl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ritmocardyl, including repackagers and relabelers. The FDA regulates Ritmocardyl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ritmocardyl 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 Ritmocardyl supplier is an individual or a company that provides Ritmocardyl active pharmaceutical ingredient (API) or Ritmocardyl finished formulations upon request. The Ritmocardyl suppliers may include Ritmocardyl API manufacturers, exporters, distributors and traders.
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A Ritmocardyl written confirmation (Ritmocardyl WC) is an official document issued by a regulatory agency to a Ritmocardyl manufacturer, verifying that the manufacturing facility of a Ritmocardyl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ritmocardyl APIs or Ritmocardyl finished pharmaceutical products to another nation, regulatory agencies frequently require a Ritmocardyl WC (written confirmation) as part of the regulatory process.
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