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Phenylephrine + Chlorpheniramine Caplet bulk supplier for pharma manufacturers

Phenylephrine + Chlorpheniramine Caplet Suppliers & Bulk Manufacturers

Available Forms: Caplet

Available Strengths: Phenylephrine HCl(10 mg); Chlorpheniramine Maleate(4 mg)

Reference Brands: Dimetapp® Cold & Allergy(US); Actifed®, Sinutab®, or Coldrex®(EU)

Category: Allergy Medication

Pharma B2B platforms in the US and EU connect global buyers and suppliers for APIs, formulations, and CDMO services. Marketplaces like Pharmatradz.com ensure verified sourcing, compliance, and seamless trade across regulated markets. Ideal for pharma importers, exporters, and distributors seeking growth in high-demand regions.

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📘 Sourcing Guide

Product Description:

Pharma B2B marketplaces in the US and EU are transforming how pharmaceutical businesses connect, trade, and grow globally. These platforms simplify sourcing of APIs, finished formulations, and contract manufacturing by offering verified suppliers, regulatory compliance, and secure transactions. With increasing demand for transparent, efficient, and GMP-compliant sourcing, B2B pharma portals like Pharmatradz.com are bridging gaps between buyers and sellers. Whether you are a wholesaler, distributor, or manufacturer, Pharma B2B solutions offer scalable opportunities across regulated markets. Join the global supply chain and explore trusted pharma trading options in the United States and European Union today.

Phenylephrine + Chlorpheniramine Caplet — third party manufacturing & bulk supply

Phenylephrine + Chlorpheniramine Caplet is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.
Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.
Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

What to include when you enquire

  • Destination market — determines which manufacturers hold the right site-level approvals
  • First order quantity and estimated annual volume
  • Whether you need a registration dossier or the product is already registered
  • Packaging, labelling and language requirements
  • Incoterms and required shelf life

Manufacturers of Phenylephrine + Chlorpheniramine Caplet listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding. Narcotic drugs and controlled substances are supplied strictly against valid import and export permits issued by the competent authorities.

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Frequently Asked Questions

Phenylephrine + Chlorpheniramine is used to relieve symptoms of cold, allergy, hay fever, and sinus congestion. It helps reduce nasal congestion, runny nose, sneezing, and watery eyes. Phenylephrine works as a decongestant that narrows blood vessels in the nasal passages, while Chlorpheniramine is an antihistamine that reduces allergic symptoms.

This combination is made from Phenylephrine hydrochloride, a nasal decongestant, and Chlorpheniramine maleate, an antihistamine that helps manage allergic responses.

The common trade names of this combination include Actifed, Sinutab, and Codral Cold & Flu.

Phenylephrine + Chlorpheniramine combinations are manufactured by several pharmaceutical companies worldwide, including Johnson & Johnson, GlaxoSmithKline (GSK), and local licensed producers.

The generic name of this medicine is Phenylephrine hydrochloride and Chlorpheniramine maleate.

The brand names of Phenylephrine + Chlorpheniramine include Actifed, Sinutab, and Codral Cold & Flu.

Phenylephrine + Chlorpheniramine combinations are manufactured in the United States, the United Kingdom, India, and several other countries under GMP-certified pharmaceutical facilities.

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