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Nicotine Patch bulk supplier for pharma manufacturers

Nicotine Patch Suppliers & Bulk Manufacturers

Available Forms: Patches

Available Strengths: 7 mg, 14 mg, 21 mg patches

Reference Brands: Nicoderm CQ

Category: Transdermal Patches

Nicotine patches release controlled nicotine to stimulate brain receptors, reducing withdrawal symptoms and cravings. They support smoking cessation, improve health, and lower addiction risks. Benefits include gradual dose reduction, fewer withdrawal symptoms, increased success rates, and safer withdrawal support, aiding long-term quitting efforts. Nicotine Patch is available in Patches and strengths such as 7 mg, 14 mg, 21 mg patches. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Nicotine Patch is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.

Technical Specifications & Supply Details
Lead Time 7 to 60 days (depending on batch size & schedule)
MOQ As per manufacturer’s batch size
COA Available with every batch
Regulatory Dossier / DMF Available upon request
Export Documentation FSC, COA, Manufacturing License, Product Permission
Standards IP, BP, USP
Certifications WHO-GMP, EU-GMP, USFDA (as applicable)

Nicotine Patch can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.

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📘 Sourcing Guide

Product Description:

Nicotine patches in the EU and US are regulated as medical devices supporting smoking cessation. In the US, FDA approval involves validation, safety validation, and GMP standards. In the EU, CE marking certifies conformity under MDR standards. These products undergo validation, stability testing, and audits, supported by detailed dossiers including safety profiles, clinical trial data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to safe, effective nicotine replacement therapy devices, supporting smoking cessation efforts worldwide, reducing tobacco-related health risks, and promoting healthier lifestyles through regulated, high-quality products.

Disclaimer: By continuing to browse, you agree to the terms of use of this website and the Trade Marks displayed, in compliance with the provisions of the Trademark Act, 1999, Section 30 and 30(1) under 'Fair use.'

The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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Frequently Asked Questions

Nicotine in pharmaceutical form is used to help people stop smoking by reducing withdrawal symptoms and cravings associated with nicotine dependence. It is commonly used as part of nicotine replacement therapy programs along with behavioral support to improve smoking cessation success rates.

Nicotine medicines contain the active ingredient nicotine or nicotine polacrilex, which is a purified form of nicotine used in controlled doses. The formulation may include excipients such as flavoring agents, stabilizers, and base materials depending on the dosage form such as gum, lozenge, patch, or spray.

Common trade names include Nicorette, Nicoderm CQ, Commit, NiQuitin, Nicotinell, and Nicotex along with other regional generic brands.

Nicotine replacement therapy products are manufactured by several pharmaceutical companies globally, including Johnson & Johnson (Nicorette / Nicoderm CQ in some markets) and GlaxoSmithKline (NiQuitin), along with many approved generic manufacturers.

The generic name is nicotine (nicotine polacrilex or nicotine base depending on the formulation).

Examples of brand names include Nicorette, Nicoderm CQ, Commit, NiQuitin, Nicotinell, and Nicotex.

Nicotine replacement therapy products are manufactured in several countries including the United States, United Kingdom, various European countries, India, and other regulated pharmaceutical manufacturing hubs depending on the marketing authorization holder and manufacturer.

Yes, Nicotine Patch is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Nicotine Patch is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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