Description

Flurbiprofen Sodium (200 Mg) is the sodium salt form of the non-steroidal anti-inflammatory drug (NSAID) flurbiprofen. This high-purity active pharmaceutical ingredient (API) is critical for ensuring the efficacy, stability, and batch-to-batch consistency of finished pharmaceutical formulations. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of analgesic and anti-inflammatory medications.

Application

• Pharmaceutical API: Primary use as the active ingredient in the manufacture of solid oral dosage forms (e.g., tablets, capsules) and sterile injectable solutions.
• Analgesic Formulations: Used in medications for the relief of mild to moderate pain, including post-operative and dental pain.
• Anti-inflammatory Therapies: Key component in drugs for managing inflammation associated with conditions like osteoarthritis and rheumatoid arthritis.
• Ophthalmic Solutions: Potential use in the formulation of eye drops for treating inflammation following cataract surgery.
• Research & Development: Serves as a reference standard and a key intermediate in preclinical and clinical research for novel NSAID delivery systems.
• Generic Drug Manufacturing: Essential for producing bioequivalent generic versions of branded flurbiprofen sodium medications.

Basic Information

Product Name	Flurbiprofen Sodium (200 Mg)
CAS No.	56767-76-1
Molecular Formula	C15H12FNaO2
Molecular Weight	266.24 g/mol
Synonyms	Flurbiprofen Sodium Salt; (±)-Flurbiprofen Sodium; 2-Fluoro-α-methyl-4-biphenylacetic Acid Sodium Salt; (RS)-Flurbiprofen Sodium; Flurbiprofen Na; Ansaid (brand name salt form); Cebutid (brand name salt form); Froben Sodium
EINECS	Contact for details

Quality Control

Our Flurbiprofen Sodium is manufactured under strict quality management systems. Each batch is tested to ensure it meets high-purity standards suitable for pharmaceutical use, with specifications typically aligned with major pharmacopoeial guidelines. A comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles is provided with every shipment to guarantee supply reliability and regulatory compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.