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01 1Dr. Reddy's Laboratories Limited

02 1Malladi Drugs & Pharmaceuticals Limited

03 1Moehs Catalana SL

04 1AURORE PHARMACEUTICALS PRIVATE LIMITED

05 1AX Pharmaceutical Corp

06 1Arene Life Sciences Private Limited

07 1Aurobindo Pharma Limited

08 1Cadila Pharmaceuticals Limited

09 1Cipla Ltd.

10 1DARMERICA, LLC

11 1Fagron Inc

12 1Glochem Industries Private Limited

13 1Hetero Drugs Limited

14 1Ipca Laboratories Limited

15 1MYLAN LABORATORIES LIMITED

16 1Medisca Inc.

17 1Novartis Pharmaceuticals Corporation

18 1Pfizer Asia Manufacturing Pte Ltd

19 1Professional Compounding Centers of America dba PCCA

20 1Spectrum Laboratory Products, Inc.

21 1Srini Pharmaceuticals Private Limited

22 1Tianish Laboratories Private Limited

23 1Unichem Laboratories Limited, India

24 1Viatris Pharmaceuticals LLC

25 1Xenex Laboratories Inc

26 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.

27 1Zydus Lifesciences Limited

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

AMLODIPINE BESYLATE

NDC Package Code : 55111-025

Start Marketing Date : 2003-03-19

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMalladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.

AMLODIPINE BESYLATE

NDC Package Code : 57218-936

Start Marketing Date : 2017-08-07

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Malladi

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMoehs Group, a reference company in the production of pharmaceutical active ingredients.

AMLODIPINE BESYLATE

NDC Package Code : 52932-0723

Start Marketing Date : 2010-07-23

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Moehs Iberica

04

CRS
Not Confirmed
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CRS
Not Confirmed

AMLODIPINE BESYLATE

NDC Package Code : 53104-7561

Start Marketing Date : 2016-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (35kg/35kg)

Marketing Category : BULK INGREDIENT

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05

CRS
Not Confirmed
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CRS
Not Confirmed

AMLODIPINE BESYLATE

NDC Package Code : 51552-1438

Start Marketing Date : 2012-04-01

End Marketing Date : 2027-02-27

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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06

CRS
Not Confirmed
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07

CRS
Not Confirmed
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CRS
Not Confirmed

AMLODIPINE BESYLATE

NDC Package Code : 38779-2734

Start Marketing Date : 2014-05-23

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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09

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CRS
Not Confirmed

AMLODIPINE BESYLATE

NDC Package Code : 51927-0073

Start Marketing Date : 2020-04-21

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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Looking for 111470-99-6 / Amlodipine Besylate API manufacturers, exporters & distributors?

Amlodipine Besylate manufacturers, exporters & distributors 1

92

PharmaCompass offers a list of Amlodipine Besylate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Amlodipine Besylate manufacturer or Amlodipine Besylate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Amlodipine Besylate manufacturer or Amlodipine Besylate supplier.

PharmaCompass also assists you with knowing the Amlodipine Besylate API Price utilized in the formulation of products. Amlodipine Besylate API Price is not always fixed or binding as the Amlodipine Besylate Price is obtained through a variety of data sources. The Amlodipine Besylate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Amlodipine Besylate

Synonyms

111470-99-6, Amlodipine besilate, Amlodipine benzenesulfonate, Antacal, Monopina, Istin

Cas Number

111470-99-6

Unique Ingredient Identifier (UNII)

864V2Q084H

About Amlodipine Besylate

A long-acting dihydropyridine calcium channel blocker. It is effective in the treatment of ANGINA PECTORIS and HYPERTENSION.

LOTREL Manufacturers

A LOTREL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LOTREL, including repackagers and relabelers. The FDA regulates LOTREL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LOTREL 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 LOTREL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

LOTREL Suppliers

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

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

LOTREL NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing LOTREL as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for LOTREL API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture LOTREL as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain LOTREL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a LOTREL NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of LOTREL suppliers with NDC on PharmaCompass.

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.