Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1Nuray Chemicals Private Limited
02 1Dr. Reddy's Laboratories Limited
03 1Malladi Drugs & Pharmaceuticals Limited
04 1Moehs Catalana SL
05 1AURORE PHARMACEUTICALS PRIVATE LIMITED
06 1AX Pharmaceutical Corp
07 1Arene Life Sciences Private Limited
08 1Aurobindo Pharma Limited
09 1Cadila Pharmaceuticals Limited
10 1Cipla Ltd.
11 1DARMERICA, LLC
12 1Fagron Inc
13 1Glochem Industries Private Limited
14 1Hetero Drugs Limited
15 1Ipca Laboratories Limited
16 1MYLAN LABORATORIES LIMITED
17 1Medisca Inc.
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
01 9AMLODIPINE BESYLATE
02 16Amlodipine Besylate
03 1Amlodipine Besylate (Process 1)
04 1Amlodipine Besylate Anhydrous
01 2Canada
02 1China
03 15India
04 1Netherlands
05 1Spain
06 6U.S.A
07 1United Kingdom
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-068
Start Marketing Date : 2019-02-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-936
Start Marketing Date : 2017-08-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
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
NDC Package Code : 53104-7561
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
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...
NDC Package Code : 24234-0009
Start Marketing Date : 2014-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2734
Start Marketing Date : 2014-05-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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...
NDC Package Code : 49452-0429
Start Marketing Date : 2015-06-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Amlodipine Besylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amlodipine Besylate, including repackagers and relabelers. The FDA regulates Amlodipine Besylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amlodipine Besylate 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 Amlodipine Besylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amlodipine Besylate supplier is an individual or a company that provides Amlodipine Besylate active pharmaceutical ingredient (API) or Amlodipine Besylate finished formulations upon request. The Amlodipine Besylate suppliers may include Amlodipine Besylate API manufacturers, exporters, distributors and traders.
click here to find a list of Amlodipine Besylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Amlodipine Besylate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Amlodipine Besylate API and other APIs are published in this directory by the FDA.
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 Amlodipine Besylate 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.
The NDC directory also contains data on finished compounded human drug products that contain Amlodipine Besylate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Amlodipine Besylate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Amlodipine Besylate suppliers with NDC on PharmaCompass.
We have 26 companies offering Amlodipine Besylate
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