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Pharmaceutical Oxacillin Sodium for Injection 500mg
US$0.078
100,000 vial
Sample price:US$2.00/vial.Request sample

Product profile

Customization

Available

Application

Internal Medicine

Usage Mode

For external use

Model NO.

500mg

Suitable for

Elderly, Children, Adult

State

Solid

Shape

Powder

Type

Organic Chemicals

Pharmaceutical Technology

Chemical Synthesis

Drug Reg./Approval No.

Lu20160062

Drug Ad Approval No.

Lu20160062

Certificate

GMO, SGS, ISO

Transport Package

10vials/Tray/Box, 50vials/Tray/Box.

Specification

500mg

Trademark

Reyoung

Origin

China

HS Code

3003909090

Production Capacity

5millions

Key features

Global Market Presence: Products marketed in over 80 countries with 35+ years of export experience.
High Production Capacity: Annual capacity includes 2 billion vials of powder for injection and 10 billion tablets.
International Certifications: Passed ISO9001, ISO14001, OHS18001, and inspections by multiple national health authorities.
OEM and ODM Services: Accepts OEM, contract manufacturing, and ODM services for custom production needs.
Professional Registration Team: Dedicated team provides necessary documents and samples for drug registration processes.
Diverse Product Portfolio: Covers antibiotics, analgesics, vitamins, anti-cancer, and cardiovascular drugs.
Established Manufacturer: Company established in 1966 with 5000 staff and 30 workshops.
Quality Assurance: Products certified by GMO, SGS, and ISO standards for international compliance.

Company profile

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableExport Year: 1997-01-01 CertifiedNearest Port: Qingdao PortAverage Response Time: ≤24h CertifiedTerms of Payment: LC, T/T, D/P

AI-Powered supplier vetting

SummaryREYOUNG PHARMACEUTICAL CO., LTD. is a China-based limited company established in 1998, with 4,950 employees and operations in Shandong. The supplier reports ISO 9001, ISO 14001, and OHSAS 18001 certifications, more than 10 production lines, 50 quality-control staff, and 370 years of combined R&D-engineer experience. Its stated manufacturing portfolio includes sterile raw materials, powders and liquids for injection, tablets, and capsules, with reported annual production above the stated threshold. The company identifies three factories, an extensive manufacturing area, international business since 1997, and export markets across South America, Africa, Southeast Asia, and the Middle East. Trade records show transactions involving India, Bolivia, and Vietnam, including cefotaxime-related products. Evidence is insufficient to assess after-sales service, financial credibility, innovation output, or customization capability. Customer-case evidence is limited to named buyers and trade records.
Supplier typeThe supplier is identified as a combined business entity and a limited company headquartered in Shandong, China. Its business scope is health and medicine, with products including sterile raw materials, injectable products, tablets, and capsules, supporting classification as a pharmaceutical manufacturer and distributor.
CertificationsThe supplier explicitly reports ISO 9001:2015, ISO 14001:2015, and OHSAS 18001:2007 certificates, and separately describes itself as GMP and ISO authenticated. These stated certifications provide direct evidence of formal quality, environmental, and occupational-health management systems.
Production capacityProduction capacity is supported by more than 10 production lines, three factories, a reported manufacturing area of 1,000,000 square meters, and stated annual output across small-volume injections, powder injections, tablets, and capsules. The supplier also reports annual production above the stated threshold, indicating substantial multi-form pharmaceutical manufacturing capability.
Client casesTrade records identify transactions involving STERILE INDIA PRIVATE LIMITED, HEREDIA ARACENA RENY EVELIN, and a Vietnam-related registration, with products including cefotaxime-related material and oral rehydration products. These records demonstrate some international commercial activity, but the evidence is limited and does not establish long-term customer performance or a broad verified customer portfolio.

Product Q&A

Q:What is the production capacity for powder for injection?
A:
The annual production capacity for powder for injection is 2 billion vials.
Q:Does the company offer OEM or ODM services?
A:
Yes, we accept OEM, contract manufacturing, and ODM services.
Q:Which international certifications has the company passed?
A:
We have passed ISO9001, ISO14001, OHS18001, and inspections by health authorities in Ethiopia, Yemen, Iraq, and others.
Q:What is the lead time for orders?
A:
The average lead time is 1-3 months for both peak and off-peak seasons.
Q:Can you assist with drug registration documentation?
A:
Yes, our professional team is responsible for registration and can provide documents and samples.

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