Description

Prednisolone, Anhydrous, Micronized USP

Prednisolone, Anhydrous, Micronized USP is a high-purity corticosteroid used in pharmaceutical formulations for its potent anti-inflammatory and immunosuppressive effects. The micronized, anhydrous form enhances dissolution, bioavailability, and uniformity in oral, topical, and compounded dosage forms. It meets United States Pharmacopeia (USP) standards for purity, potency, and particle size. Prednisolone, Anhydrous is
• A USP-compliant corticosteroid with anti-inflammatory and immunosuppressive properties
• Micronized for improved solubility, uniform dispersion, and enhanced bioavailability
• Used in oral tablets, capsules, suspensions, and compounded topical formulations
• Suitable for acute and chronic inflammatory conditions, autoimmune disorders, and allergic reactions
• Manufactured under Good Manufacturing Practice (GMP) conditions
• Supplied with complete regulatory documentation including Certificate of Analysis (CoA) and technical data
Prednisolone, Anhydrous, Micronized USP is chemically designated as 11β,17α,21-Trihydroxy-pregna-1,4-diene-3,20-dione. It appears as a white to off-white fine crystalline powder, with high purity and controlled particle size to optimize dissolution and formulation consistency.
In pharmaceutical applications, Prednisolone, Anhydrous, Micronized USP is used in:
• Oral tablets and capsules for systemic anti-inflammatory therapy
• Compounded suspensions and oral solutions for accurate dosing in pediatric or elderly patients
• Topical creams, gels, and ointments for localized anti-inflammatory effects
• Combination products with other actives to enhance therapeutic efficacy
• Research and clinical formulations requiring reproducible particle size and consistent dissolution
The micronized, anhydrous form improves the pharmacokinetic profile of prednisolone, enabling rapid absorption and predictable onset of action. Its high purity ensures minimal variability in formulation performance.
CarboMer supplies Prednisolone, Anhydrous, Micronized USP with control over assay, particle size distribution, residual solvents, and microbial content. Each batch meets USP monograph specifications and is suitable for regulated pharmaceutical use.
The material is packaged in sealed, moisture-protective, tamper-evident containers. Available in laboratory, pilot, and commercial-scale quantities. Minimum order quantities (MOQ), lead times, and documentation including CoA and SDS are provided upon request.
Each batch is tested for identity (IR, HPLC), assay (anhydrous basis), particle size, residual solvents, heavy metals, and microbial purity. Certificates of Analysis (CoA), Safety Data Sheets (SDS), and full traceability documentation accompany every shipment.
As with all CarboMer corticosteroid APIs, Prednisolone, Anhydrous, Micronized USP is supported by formulation expertise, regulatory guidance, and reliable global supply to help develop safe, effective, and compliant pharmaceutical products.