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01 1ANUH PHARMA LIMITED

02 1DARMERICA, LLC

03 1Fagron Inc

04 1Galenova Inc

05 1Jiangsu Lianhuan Pharmaceutical Co.,Ltd.

06 1LETCO MEDICAL, LLC

07 1Medisca Inc.

08 1Nanjing White Whale Pharmaceutical Co., Ltd

09 1Professional Compounding Centers of America

10 2Quimica Sintetica S.A.

11 1Reliable Biopharmaceutical LLC

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PharmaCompass

01

AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 64677-0002

Start Marketing Date : 2018-04-02

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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02

AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 71052-687

Start Marketing Date : 2021-08-10

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1000g/1000g)

Marketing Category : BULK INGREDIENT

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03

AACR Annual meeting
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AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 51552-1419

Start Marketing Date : 2021-10-15

End Marketing Date : 2027-02-28

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

Marketing Category : BULK INGREDIENT

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04

AACR Annual meeting
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AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 62991-1031

Start Marketing Date : 2009-07-01

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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05

AACR Annual meeting
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AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 38779-0203

Start Marketing Date : 2014-07-07

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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06

AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 51927-0214

Start Marketing Date : 2021-09-24

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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07

AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 53069-0920

Start Marketing Date : 1999-02-28

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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08

AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 53069-0010

Start Marketing Date : 1999-02-28

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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09

AACR Annual meeting
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CHLORAMPHENICOL

NDC Package Code : 59605-7806

Start Marketing Date : 2014-01-08

End Marketing Date : 2025-05-18

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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10

Nanjing White Whale Pharmaceutical ...

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Nanjing White Whale Pharmaceutical ...

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CHLORAMPHENICOL

NDC Package Code : 66478-0155

Start Marketing Date : 2013-12-02

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 56-75-7 / Chloramphenicol API manufacturers, exporters & distributors?

Chloramphenicol manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Chloramphenicol

Synonyms

56-75-7, Chloromycetin, Chlornitromycin, Levomycetin, Chloroamphenicol, Halomycetin

Cas Number

56-75-7

Unique Ingredient Identifier (UNII)

66974FR9Q1

About Chloramphenicol

An antibiotic first isolated from cultures of Streptomyces venequelae in 1947 but now produced synthetically. It has a relatively simple structure and was the first broad-spectrum antibiotic to be discovered. It acts by interfering with bacterial protein synthesis and is mainly bacteriostatic. (From Martindale, The Extra Pharmacopoeia, 29th ed, p106)

Chlorsig Manufacturers

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

Chlorsig Suppliers

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

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

Chlorsig 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 Chlorsig as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Chlorsig Manufacturers | Traders | Suppliers

Chlorsig 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.