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Ibuprofen
API

Ibuprofen grades are available to suit a wide array of pharmaceutical forms, considering its crystalline nature

HUMAN API

Ibuprofen

Ibuprofen is a fundamental Active Pharmaceutical Ingredient (API) belonging to the Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) class. It is distinguished by its triple action: Analgesic (pain relief), Antipyretic (fever reduction), and Anti-inflammatory effects. We supply Ibuprofen in high-purity grades, including specialized grades to ensure optimal formulation efficiency and stability across various pharmaceutical dosage forms.

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).
Therapeutic Class:
Non-Steroidal Anti-Inflammatory Drug (NSAID).
Mechanism of Action:
Inhibits Cyclooxygenase enzymes (COX-1 and COX-2), thereby reducing the production of prostaglandins responsible for pain, inflammation, and fever.
Clinical Application:
Treatment of mild to moderate pain, and inflammation associated with conditions such as arthritis, muscle pain, migraines, and dysmenorrhea (menstrual pain).
Competitive Advantage:
High efficacy in managing symptoms requiring anti-inflammatory action, in addition to pain relief and fever reduction.
Tablets and Capsules

Film-coated tablets, immediate-release, and fast-dissolving tablets.

Supplied in grades with excellent flowability to facilitate high-speed automated filling and direct compression processes.

Liquid Formulations

Suspensions and pediatric syrups.

Purity grade ensures chemical stability and prevents degradation in liquid media, with a focus on minimizing bitter taste.

Topical Preparations

Gels and creams for localized pain relief.

Availability of grades with optimal solubility in commonly used gel and cream bases.

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).

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