DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddys Laboratories Limited
02 1M/S Sai Tech Pharmaceuticals Pvt Ltd
03 1M/s Aarti Drugs Ltd
04 1M/s Aurore Pharmaceuticals Private Limited
05 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
06 1M/s. Cadila Pharmaceuticals Ltd.,
07 1M/s. Glochem Industries Ltd
08 1M/s. Hetero Drugs Limited
09 1M/s. Apotex Pharmachem India Pvt. Ltd.,
01 1Raloxefene hydrochloride Ph.Eur/USP
02 1Raloxifene Hydrochloride (IH/USP/Ph.Eur)
03 2Raloxifene Hydrochloride (USP)
04 1Raloxifene Hydrochloride (USP/EP)
05 1Raloxifene Hydrochloride EP
06 1Raloxifene Hydrochloride EP/IH/USP
07 1Raloxifene Hydrochloride USP/EP
08 1Raloxifene Rizatriptan ro Hydchloride (Ph. Eur)
01 1WC-0023
02 1WC-0029
03 1WC-0034
04 1WC-0066
05 1WC-0074
06 1WC-0119
07 1WC-0128
08 1WC-0219
09 1WC-0422
01 9India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Raloxifene Hydrochloride (IH/USP/Ph.Eur)
Date of Issue : 2022-06-15
Valid Till : 2025-06-16
Written Confirmation Number : WC-0034
Address of the Firm : Chemical Technical Operations-Unit II, Plot Nos. 1, 75A, 75B, 105, 110, 111 & 1...
Date of Issue : 2022-08-10
Valid Till : 2025-08-05
Written Confirmation Number : WC-0219
Address of the Firm : Plot No. E-22, MIDC Tarapur-Boisar, Thane-401506, Maharashtra
Raloxifene Hydrochloride (USP/EP)
Date of Issue : 2014-03-06
Valid Till : 2016-07-02
Written Confirmation Number : WC-0128
Address of the Firm : 1A, Bommasandra Industrial Area, 4th Phase,Bommasandra Industrial Estate (Post O...
Raloxifene Rizatriptan ro Hydchloride (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...
Raloxefene hydrochloride Ph.Eur/USP
Date of Issue : 2022-09-19
Valid Till : 2025-07-02
Written Confirmation Number : WC-0119
Address of the Firm : Plot No. 35, 36, 38, 39,40,49, 50 & 51, Phase-IV, IDA, Jeedimetla, Medchal- Malk...
Raloxifene Hydrochloride (USP)
Date of Issue : 2022-09-01
Valid Till : 2025-07-02
Written Confirmation Number : WC-0074
Address of the Firm : 294, GIDC Estate, Ankleshwar-393 002, Bharuch, Gujarat, India
Raloxifene Hydrochloride EP/IH/USP
Date of Issue : 2013-06-11
Valid Till : 2016-06-05
Written Confirmation Number : WC-0029
Address of the Firm : Unit-II, Sy. No. 36, 37 and 46, Plot No. 77, J. N. Pharmacity, Thanam (V), Paraw...
Raloxifene Hydrochloride (USP)
Date of Issue : 2019-08-09
Valid Till : 2025-08-08
Written Confirmation Number : WC-0066
Address of the Firm : Plot No. 1, Hetero SEZ Infrastructure Ltd., Narasapuram, Visakhapatnam-531 081, ...
Raloxifene Hydrochloride USP/EP
Date of Issue : 2018-06-08
Valid Till : 2021-06-07
Written Confirmation Number : WC-0422
Address of the Firm : Plot No. A-145/8, Khairane, M.I.D.C. Industrial Area, Navi Mumbai - 400 705, Tal...
A Evista manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Evista, including repackagers and relabelers. The FDA regulates Evista manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Evista 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 Evista manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Evista supplier is an individual or a company that provides Evista active pharmaceutical ingredient (API) or Evista finished formulations upon request. The Evista suppliers may include Evista API manufacturers, exporters, distributors and traders.
click here to find a list of Evista suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Evista written confirmation (Evista WC) is an official document issued by a regulatory agency to a Evista manufacturer, verifying that the manufacturing facility of a Evista active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Evista APIs or Evista finished pharmaceutical products to another nation, regulatory agencies frequently require a Evista WC (written confirmation) as part of the regulatory process.
click here to find a list of Evista suppliers with Written Confirmation (WC) on PharmaCompass.
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