Your Trusted Source for GMP-Certified Drug Components.

Acetaminophen
Paracetamol

We offer Paracetamol grades adapted for various manufacturing techniques

HUMAN APIs

Paracetamol

Paracetamol (Acetaminophen) is one of the most widely used Active Pharmaceutical Ingredients (APIs globally). It belongs to the analgesic and antipyretic class, serving as a foundational substance with a wide safety margin when used at recommended doses. We supply Paracetamol in high-purity grades to ensure ease of formulation and compliance with international regulatory standards.

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).
A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.
A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.
Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).
g
Therapeutic Class:
Analgesic (Pain Reliever) and Antipyretic (Fever Reducer)..
Mechanism of Action:
Believed to primarily inhibit prostaglandin synthesis in the Central Nervous System (CNS), resulting in pain relief and fever reduction.
Clinical Application:
Treatment of mild to moderate pain (such as headaches and dental pain), and reduction of fever associated with colds and influenza.
Competitive Advantage:
Clinically proven and safe applicability across various age groups (including pediatric and adult patients).
Tablets and Capsules

Standard oral tablets, extended-release, chewable, or effervescent tablets.

API powder supplied with optimized specifications (particle size and bulk density) for efficient Direct Compression processes.

Liquid Formulations

Syrups and suspensions for pediatric and adult use..

High purity grade ensures easy dissolution and stability within liquid matrices.

Other Preparations

Suppositories and Intravenous (IV) injections (for professional use).

Availability of customized grades to ensure physicochemical stability and compatibility with various excipients.

Regulatory Compliance

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).

Certificate of Analysis (CoA)

A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.

Drug Master File (DMF)

A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.

Manufacturing Operations

Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).

Browse Our API and Excipient Categories

4.98

488 rating

98%

Genuine client's
positive feedback.

200+

(APIs) and
Excipients.
atassco.
drug.
store.
atassco.
drug.
store.
Scroll