Your Trusted Source for GMP-Certified Drug Components.

Diclofenac Potassium
API

Diclofenac Potassium grades are available for formulations that require the fastest possible release

HUMAN API

Diclofenac Potassium

Diclofenac Potassium is a highly effective salt form of the Non-Steroidal Anti-Inflammatory Drugs (NSAIDs) class, and it is the preferred choice for Fast-Acting formulations. This salt is characterized by its very high water solubility compared to Diclofenac Sodium, which ensures rapid absorption and faster pain relief. We supply Diclofenac Potassium with high quality and purity, making it ideal for manufacturing rapid-onset tablets and formulations that require immediate action.

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:
NSAID - Rapid Onset of Action.
Mechanism of Action:
Inhibits Cyclooxygenase enzymes (COX-1 and COX-2), reducing the synthesis of prostaglandins responsible for pain and inflammation.
Clinical Application:
Management of acute pain conditions requiring quick relief, such as dental pain, migraine attacks, post-operative pain, and dysmenorrhea (menstrual pain).
Competitive Advantage:
The Superior Solubility of the potassium salt translates into rapid gastrointestinal absorption, offering the fastest onset of action among diclofenac salts.
Rapid Release Tablets

Coated or uncoated tablets designed for immediate absorption.

High API solubility reduces the need for expensive disintegrants and ensures reliable drug release.

Oral Powder/Sachets

Powder to be dissolved in water or taken directly for super-fast absorption.

Excellent powder properties for high-precision, automated filling processes into sachets.

Liquid Formulations

Concentrated oral solutions.

Rapid and complete dissolution of the potassium salt in aqueous media.

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