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01 1Virupaksha Organics

02 2Dr. Reddy's Laboratories

03 1Granules India Limited

04 2TAPI Technology & API Services

05 1Aurobindo Pharma Limited

06 1Chemeca Drugs

07 1Cipla

08 3Dipharma

09 1Hetero Drugs

10 1Ind Swift Laboratories Limited

11 1Jubilant Generics

12 1Morepen Laboratories

13 1Perrigo API India Private Limited

14 1RANBAXY LABORATORIES LIMITED

15 1THINQ Pharma-CRO PVT Ltd

16 1Vasudha Pharma Chem

17 1Viatris

18 2Wockhardt

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWith Virupaksha, you get a quality product with on-time delivery.

GDUFA

DMF Review : Complete

Rev. Date : 2014-07-15

Pay. Date : 2014-06-27

DMF Number : 23070

Submission : 2009-08-10

Status : Active

Type : II

Virupaksha

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

GDUFA

DMF Review : Complete

Rev. Date : 2020-12-12

Pay. Date : 2020-12-04

DMF Number : 15757

Submission : 2001-12-05

Status : Active

Type : II

Dr Reddy Company Banner

03

PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothGranules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

GDUFA

DMF Review : Complete

Rev. Date : 2016-09-19

Pay. Date : 2016-07-12

DMF Number : 30604

Submission : 2016-08-16

Status : Active

Type : II

Granules India

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 18948

Submission : 2005-11-09

Status : Inactive

Type : II

TAPI Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

GDUFA

DMF Review : Complete

Rev. Date : 2020-04-15

Pay. Date : 2020-03-26

DMF Number : 34645

Submission : 2020-03-12

Status : Active

Type : II

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI offers customized CDMO Solutions for API development and manufacturing services.

GDUFA

DMF Review : N/A

Rev. Date :

Pay. Date :

DMF Number : 18949

Submission : 2005-11-09

Status : Inactive

Type : II

TAPI Company Banner

Fexofenadine Hydrochloride Manufacturers

A Fexofenadine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fexofenadine Hydrochloride, including repackagers and relabelers. The FDA regulates Fexofenadine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 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.

click here to find a list of Fexofenadine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Fexofenadine Hydrochloride Suppliers

A Fexofenadine Hydrochloride supplier is an individual or a company that provides Fexofenadine Hydrochloride active pharmaceutical ingredient (API) or Fexofenadine Hydrochloride finished formulations upon request. The Fexofenadine Hydrochloride suppliers may include Fexofenadine Hydrochloride API manufacturers, exporters, distributors and traders.

click here to find a list of Fexofenadine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Fexofenadine Hydrochloride USDMF

A Fexofenadine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Fexofenadine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Fexofenadine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Fexofenadine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.

A Fexofenadine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Fexofenadine Hydrochloride USDMF includes data on Fexofenadine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Fexofenadine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.

click here to find a list of Fexofenadine Hydrochloride suppliers with USDMF on PharmaCompass.

Fexofenadine Hydrochloride Manufacturers | Traders | Suppliers

Fexofenadine Hydrochloride Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.