Inabata Inabata


Find Amlodipine manufacturers, exporters & distributors on PharmaCompass

API Suppliers

API Suppliers

US DMFs Filed

US DMFs Filed

CEP/COS Certifications

CEP/COS Certifications


JDMFs Filed

JDMFs Filed




Listed Suppliers

Listed Suppliers

USA (Orange Book)

USA (Orange Book)









South Africa

South Africa

Uploaded Dossiers

Uploaded Dossiers


U.S. Medicaid


Annual Reports


USFDA Orange Book Patents


USFDA Exclusivities



Blog #PharmaFlow








Other Listed Suppliers


Looking for 88150-42-9 / Amlodipine API manufacturers, exporters & distributors?

Amlodipine manufacturers, exporters & distributors 1


PharmaCompass offers a list of Amlodipine 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 manufacturer or Amlodipine supplier for your needs.

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

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

API | Excipient name



88150-42-9, Norvasc, Amlodipine base, Amlodipino, Amlodipinum, Caduet

Cas Number


Unique Ingredient Identifier (UNII)


About Amlodipine

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

Amlodipine Manufacturers

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

Amlodipine Suppliers

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

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

Amlodipine USDMF

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

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

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

Amlodipine JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The Amlodipine Drug Master File in Japan (Amlodipine JDMF) empowers Amlodipine API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the Amlodipine JDMF during the approval evaluation for pharmaceutical products. At the time of Amlodipine JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of Amlodipine suppliers with JDMF on PharmaCompass.

Amlodipine KDMF

In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

Pharmaceutical companies submit a Amlodipine Drug Master File in Korea (Amlodipine KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Amlodipine. The MFDS reviews the Amlodipine KDMF as part of the drug registration process and uses the information provided in the Amlodipine KDMF to evaluate the safety and efficacy of the drug.

After submitting a Amlodipine KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Amlodipine API can apply through the Korea Drug Master File (KDMF).

click here to find a list of Amlodipine suppliers with KDMF on PharmaCompass.

Amlodipine 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 Amlodipine as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Amlodipine 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 Amlodipine 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 Amlodipine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Amlodipine NDC to their finished compounded human drug products, they may choose to do so.

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

Amlodipine GMP

Amlodipine Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

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

Amlodipine CoA

A Amlodipine CoA (Certificate of Analysis) is a formal document that attests to Amlodipine's compliance with Amlodipine specifications and serves as a tool for batch-level quality control.

Amlodipine CoA mostly includes findings from lab analyses of a specific batch. For each Amlodipine CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Amlodipine may be tested according to a variety of international standards, such as European Pharmacopoeia (Amlodipine EP), Amlodipine JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Amlodipine USP).

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.
Ask Us for Pharmaceutical Supplier and Partner
Ask Us, Find A Supplier / Partner
No Commissions, No Strings Attached, Get Connected for FREE

What are you looking for?

How can we help you?

The request can't be empty

Please read our Privacy Policy carefully

You must agree to the privacy policy

The name can't be empty
The company can't be empty.
The email can't be empty Please enter a valid email.
The mobile can't be empty
Post Enquiry