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Looking for 86483-48-9 / Ciprofloxacin Hydrochloride API manufacturers, exporters & distributors?

Ciprofloxacin Hydrochloride manufacturers, exporters & distributors 1


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

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

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

API | Excipient name

Ciprofloxacin Hydrochloride


Ciprofloxacin hcl, 93107-08-5, 86483-48-9, 1-cyclopropyl-6-fluoro-4-oxo-7-(piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid hydrochloride, Cipro, Chebi:310388

Cas Number


Unique Ingredient Identifier (UNII)


About Ciprofloxacin Hydrochloride

A broad-spectrum antimicrobial carboxyfluoroquinoline.

Ciprofloxacin Hydrochloride Manufacturers

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

Ciprofloxacin Hydrochloride Suppliers

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

CLICK HERE to find a list of Ciprofloxacin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Ciprofloxacin Hydrochloride USDMF

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

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

CLICK HERE to find a list of Ciprofloxacin Hydrochloride suppliers with USDMF on PharmaCompass.

Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride Drug Master File in Japan (Ciprofloxacin Hydrochloride JDMF) empowers Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride suppliers with JDMF on PharmaCompass.

Ciprofloxacin Hydrochloride KDMF

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

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

After submitting a Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride API can apply through the Korea Drug Master File (KDMF).

CLICK HERE to find a list of Ciprofloxacin Hydrochloride suppliers with KDMF on PharmaCompass.

Ciprofloxacin Hydrochloride CEP

A Ciprofloxacin Hydrochloride CEP of the European Pharmacopoeia monograph is often referred to as a Ciprofloxacin Hydrochloride Certificate of Suitability (COS). The purpose of a Ciprofloxacin Hydrochloride CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Ciprofloxacin Hydrochloride EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Ciprofloxacin Hydrochloride to their clients by showing that a Ciprofloxacin Hydrochloride CEP has been issued for it. The manufacturer submits a Ciprofloxacin Hydrochloride CEP (COS) as part of the market authorization procedure, and it takes on the role of a Ciprofloxacin Hydrochloride CEP holder for the record. Additionally, the data presented in the Ciprofloxacin Hydrochloride CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Ciprofloxacin Hydrochloride DMF.

A Ciprofloxacin Hydrochloride CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Ciprofloxacin Hydrochloride CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

CLICK HERE to find a list of Ciprofloxacin Hydrochloride suppliers with CEP (COS) on PharmaCompass.

Ciprofloxacin Hydrochloride WC

A Ciprofloxacin Hydrochloride written confirmation (Ciprofloxacin Hydrochloride WC) is an official document issued by a regulatory agency to a Ciprofloxacin Hydrochloride manufacturer, verifying that the manufacturing facility of a Ciprofloxacin Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ciprofloxacin Hydrochloride APIs or Ciprofloxacin Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Ciprofloxacin Hydrochloride WC (written confirmation) as part of the regulatory process.

CLICK HERE to find a list of Ciprofloxacin Hydrochloride suppliers with Written Confirmation (WC) on PharmaCompass.

Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride as an active pharmaceutical ingredient (API).

Finished drug products

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

CLICK HERE to find a list of Ciprofloxacin Hydrochloride suppliers with NDC on PharmaCompass.

Ciprofloxacin Hydrochloride GMP

Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride 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 Ciprofloxacin Hydrochloride GMP manufacturer or Ciprofloxacin Hydrochloride GMP API supplier for your needs.

Ciprofloxacin Hydrochloride CoA

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

Ciprofloxacin Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Ciprofloxacin Hydrochloride 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.

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