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01 120181126-209-J-89
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GDUFA
DMF Review : Reviewed
Rev. Date : 2014-07-15
Pay. Date : 2014-06-27
DMF Number : 23070
Submission : 2009-08-10
Status : Active
Type : II
Certificate Number : CEP 2009-160 - Rev 05
Issue Date : 2026-04-20
Type : Chemical
Substance Number : 2280
Status : Valid
Registration Number : 307MF10001
Registrant's Address : Plot No. : B1 and B2, IDA, Gandhinagar, Kukatpally, Medchal Malkajgiri, Hyderabad, Telangana 500037, India.
Initial Date of Registration : 2025-01-09
Latest Date of Registration :
Date of Issue : 2025-10-01
Valid Till : 2028-09-30
Written Confirmation Number : WC-0191
Address of the Firm :
NDC Package Code : 51686-0001
Start Marketing Date : 2007-10-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Hiple Co., Ltd.
Registration Date : 2026-04-28
Registration Number : 20220324-209-J-1154(2)
Manufacturer Name : M/S. Virupaksha Organics Ltd
Manufacturer Address : Sy.No. 10, Gaddapothram Village, Jinnaram Mandal, Sangareddy District, Telangana State, India
Certificate Number : R1-CEP 2009-297 - Rev 03
Issue Date : 2021-12-09
Type : Chemical
Substance Number : 2280
Status : Valid
Registration Number : 302MF10017
Registrant's Address : Brueningstrasse 50, 65926 Frankfurt am Main, Germany
Initial Date of Registration : 2020-01-31
Latest Date of Registration :
NDC Package Code : 82348-104
Start Marketing Date : 1997-12-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Handok Co., Ltd.
Registration Date : 2021-04-23
Registration Number : 20210423-209-J-951
Manufacturer Name : EUROAPI Germany GmbH
Manufacturer Address : Brüningstraße 50, 65926, Frankfurt am Main, Germany
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
NDC Package Code : 58175-0616
Start Marketing Date : 2017-11-30
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-12-12
Pay. Date : 2020-12-04
DMF Number : 15757
Submission : 2001-12-05
Status : Active
Type : II
Certificate Number : CEP 2025-159 - Rev 00
Issue Date : 2025-07-08
Type : Chemical
Substance Number : 2280
Status : Valid
Registration Number : 302MF10124
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2020-10-05
Latest Date of Registration :
Date of Issue : 2025-07-25
Valid Till : 2028-06-04
Written Confirmation Number : WC-0043
Address of the Firm :
NDC Package Code : 71796-015
Start Marketing Date : 2020-03-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Sangjin Trading Co., Ltd.
Registration Date : 2022-10-06
Registration Number : 20221006-209-J-1373
Manufacturer Name : Dr. Reddy's Laboratories Ltd.
Manufacturer Address : Peddadevulapalli Village, Tripuraram Mandal, Nalgonda District, Telangana State, India - 508207
| Available Reg Filing : ASMF |
Since 1980, Octavius Pharma has been empowering lives by delivering trusted healthcare solutions, including DC granules, APIs, and FDFs
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PharmaCompass offers a list of Fexofenadine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Fexofenadine Hydrochloride manufacturer or Fexofenadine Hydrochloride supplier for your needs.
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A ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE 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 ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE supplier is an individual or a company that provides ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE active pharmaceutical ingredient (API) or ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE finished formulations upon request. The ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE suppliers may include ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
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We have 67 companies offering ALLEGRA-D COMPONENT FEXOFENADINE HYDROCHLORIDE
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