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01 1Malladi Drugs & Pharmaceuticals Limited

02 1Supriya Lifescience Limited

03 1Fagron Inc

04 1KALCHEM INTERNATIONAL INC

05 1Kongo Chemical Co., Ltd.

06 1LETCO MEDICAL, LLC

07 1Professional Compounding Centers of America

08 1SpecGx LLC

09 1Spectrum Laboratory Products, Inc.

10 1Srikem laboratories Pvt. Ltd.

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

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

CHLORPHENIRAMINE MALEATE

NDC Package Code : 57218-765

Start Marketing Date : 2017-04-18

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Malladi

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSupriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.

CHLORPHENIRAMINE MALEATE

NDC Package Code : 61281-3300

Start Marketing Date : 2013-11-20

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Supriya

03

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

CHLORPHENIRAMINE MALEATE

NDC Package Code : 51552-0137

Start Marketing Date : 1998-04-01

End Marketing Date : 2026-01-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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04

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

CHLORPHENIRAMINE MALEATE

NDC Package Code : 60592-251

Start Marketing Date : 2024-10-09

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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05

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

CHLORPHENIRAMINE MALEATE

NDC Package Code : 12294-9998

Start Marketing Date : 1978-01-21

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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06

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

CHLORPHENIRAMINE MALEATE

NDC Package Code : 62991-1032

Start Marketing Date : 1997-10-23

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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07

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE

NDC Package Code : 0406-0117

Start Marketing Date : 2013-02-11

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (.9kg/kg .0055kg/kg)

Marketing Category : DRUG FOR FURTHER PROCESSING

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08

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

CHLORPHENIRAMINE MALEATE

NDC Package Code : 51927-0247

Start Marketing Date : 2022-09-14

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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09

RDD 2025
Not Confirmed
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Looking for 113-92-8 / Chlorpheniramine Maleate API manufacturers, exporters & distributors?

Chlorpheniramine Maleate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Chlorpheniramine Maleate

Synonyms

113-92-8, Chlorphenamine maleate, Neorestamin, Synistamin, Piriton, Chlor-trimeton

Cas Number

113-92-8

Unique Ingredient Identifier (UNII)

V1Q0O9OJ9Z

About Chlorpheniramine Maleate

A histamine H1 antagonist used in allergic reactions, hay fever, rhinitis, urticaria, and asthma. It has also been used in veterinary applications. One of the most widely used of the classical antihistaminics, it generally causes less drowsiness and sedation than PROMETHAZINE.

Alka-seltzer plus Manufacturers

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

Alka-seltzer plus Suppliers

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

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

Alka-seltzer plus 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 Alka-seltzer plus as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Alka-seltzer plus suppliers with NDC on PharmaCompass.

Alka-seltzer plus Manufacturers | Traders | Suppliers

Alka-seltzer plus 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.