LLM Information

Wells Pharma

Directory listing
Pharmaceuticals 📍 Houston, TX

Directory record status

These labels describe this UNITEMFG record. They do not guarantee current capabilities, certifications, capacity, quality, or fit for a specific job.

Directory listing
Listed
Ownership
Unclaimed
Evidence reviewed
Not recorded
Last evidence review
Not recorded

About

Wells Pharma is a leading FDA-registered 503B outsourcing facility based in Houston, Texas, specializing in high-quality pharmaceutical compounding and manufacturing services. With over 100 years of combined industry experience, the company operates a state-of-the-art facility licensed to ship products to all 50 states, serving healthcare providers nationwide with reliable pharmaceutical solutions. The company focuses on critical care and pain management products, offering an extensive portfolio including OR syringes, antibiotics, pain and PCA management solutions, epidurals and nerve blocks, pre-filled Arrow pain pumps, and various non-sterile pharmaceutical products. Wells Pharma maintains rigorous FDA compliance standards and operates under strict quality control protocols to ensure product safety and efficacy. Wells Pharma distinguishes itself through automated production capabilities that enable most products to ship within 48 hours, ensuring consistent supply for healthcare facilities. The company built its reputation on five core principles: superior quality, exceptional customer service, comprehensive product offerings, consistent supply chain management, and competitive pricing structures. Their modern manufacturing facility utilizes advanced compounding technologies and follows stringent pharmaceutical manufacturing standards. Wells Pharma serves hospitals, surgery centers, and healthcare facilities across the United States, providing customized pharmaceutical solutions that meet specific clinical requirements while maintaining the highest standards of pharmaceutical manufacturing excellence.

Specialties

503B OutsourcingReady-To-Use MedicationsHospital PharmaceuticalsSterile CompoundingInjectable Medications

Manufacturing Capabilities

Processes

Sterile CompoundingInjectable ManufacturingAseptic ProcessingQuality Control

Materials

Sterile InjectablesPharmaceutical SolutionsIV Medications

Certifications & Quality

Business Certifications

FDA 503B RegistrationcGMP

Source-backed capabilities

These capability statements were observed in the linked manufacturer sources. They are source evidence, not a certification of the company or its current capacity.

Certification

  • cGMP

    and continuous improvement guide daily decision-making across all teams. Regulatory Compliance & Accreditation: Compliance is not treated as a checklist; it is embedded into our processes to ensure consistent execution, sustained regulatory alignment, and adherence to applicable cGMP requirements. Comprehensive Quality Management System (QMS): Our Quality Management System (QMS) is the backbone of how we ensure consistent, dependable product quality. It provides structured oversight of document

  • FDA 503B Registration

    lity was designed with one goal: to be a sterile compounding partner for healthcare systems in Texas and beyond. From raw material intake through final shipment, every square foot of our facility has been designed to support compliance, and process consistency. Our facility holds FDA 503B registration, DEA registration, and operates in full compliance with current Good Manufacturing Practices (cGMP) and USP <797> standards. Each operational area, from our ISO-classified cleanrooms to our q

Location

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Houston, TX •••••