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Good Quality Antibiotics Amoxicillin and Clavulanate Potassium Tablets 562.5mg
Negotiable
10,000 box

Product profile

Customization

Available

Application

Internal Medicine

Usage Mode

For oral administration

Model NO.

375mg; 562.5mg; 625mg; 1g

Suitable for

Elderly, Children, Adult

State

Solid

Shape

Tablet

Standard

Bp/ USP

Transport Package

7tabs/Blister; 10tabs/Blister

Specification

50*38*36 CM

Trademark

Reyoung

Origin

China

Production Capacity

2, 000, 000, 000 Per Year

Key features

Global GMP Certification: Passed GMP inspections in Colombia, Peru, Congo, Ethiopia, Uganda, Nigeria, Ghana, Tanzania, Kenya, Cote d'Ivoire, Pakistan, Ukraine, Philippines, Cambodia, and more.
Massive Production Capacity: Annual capacity includes 4 billion tablets, 6 billion capsules, 2.5 billion vials of powder for injection, and 2000 tons of API.
Wide Application Scope: Treats upper/lower respiratory, urinary tract, skin, and soft tissue infections, as well as otitis media and sepsis.
Established Manufacturer: Reyoung Pharma established in 1966, covering 1,000,000 sqm with over 5,000 staff and 30 workshops.
International Market Reach: Exports to over 70 countries across Asia, South America, Africa, CIS, Middle East, and Europe.
Comprehensive Product Range: Produces tablets, capsules, granules, sterile/non-sterile APIs, injections, suppositories, and traditional Chinese medicine.
Quality Certifications: Certified by GMP, ISO9001, ISO14001, and OHS18001. Recognized as a state-focused high & new tech enterprise.
Flexible Manufacturing Services: Offers OEM and ODM services with over 20 years of experience in international transactions.

Company profile

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableExport Year: 2020-10-13 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 available information identifies it as a pharmaceutical manufacturer supplying injectable antibiotics, oral solid medicines, veterinary cefotaxime sodium sterile, and lyophilized products. It reports more than 10 production lines, 370 years of combined R&D engineer experience, 50 quality-control staff, and ISO9001, ISO14001, and ISO45001 certifications. Export sales represent 31%–40% of total sales, with exporting reported since 2020 in one record and since 1998 in the company description, creating a discrepancy. Trade records show limited documented transactions and associated buyers in Bolivia, India, and Vietnam. Evidence is insufficient to assess after-sales service, financial credibility, customization, or verified customer performance comprehensively.
Supplier typeThe supplier is identified as a limited company and pharmaceutical manufacturer based in Shandong, China. Its stated products include injectable cephalosporins and penicillins, oral solid medicines, lyophilized products, and veterinary medicines, indicating a combined manufacturing and commercial business profile.
CertificationsThe supplier reports ISO9001:2015, ISO14001:2015, and ISO45001:2016 management-system certificates, along with cGMP, PIC/S, and ANVISA GMP holdings. These claims directly support established quality, environmental, occupational-safety, and pharmaceutical GMP capability, although certificate validity and scope are not independently shown.
R&D capabilityThe supplier reports 370 years of total R&D engineer experience and offers multiple dosage forms and pharmaceutical categories, including lyophilized products and injectable antibiotics. These details support R&D resources and product-development breadth, but no information confirms proprietary technologies, new product launches, patents, or development outcomes.
Production capacityProduction capability is supported by 4,950 employees, more than 10 production lines, pharmaceutical manufacturing descriptions, and product records for injectable antibiotics and veterinary cefotaxime sodium sterile. The plant-area entry is recorded as 0.0m², which is unusable or inconsistent data, so facility scale cannot be confirmed from that field.
Client casesTrade-related records associate the supplier with buyers in Bolivia, India, and Vietnam and show documented transactions for oral rehydration products, cefotaxime acid, and ceftriaxone sodium for injection. The records show some international commercial activity, but the number of stated transactions is limited and no customer testimonials, repeat-order evidence, or performance evaluations are provided.

Product Q&A

Q:What infections does this antibiotic treat?
A:
It treats upper and lower respiratory tract infections, urinary tract infections, skin and soft tissue infections, otitis media, osteomyelitis, sepsis, peritonitis, and post-operative infections.
Q:Which countries has Reyoung Pharma passed GMP inspections in?
A:
Reyoung Pharma has passed GMP inspections in Colombia, Peru, Congo, Ethiopia, Uganda, Nigeria, Ghana, Tanzania, Kenya, Cote d'Ivoire, Pakistan, Ukraine, Philippines, and Cambodia.
Q:What is the annual production capacity of the manufacturer?
A:
The annual capacity includes 4 billion tablets, 6 billion capsules, 2.5 billion vials of powder for injection, 300 million ampoules of liquid injection, and 2000 tons of API.
Q:Does the manufacturer offer OEM or ODM services?
A:
Yes, Reyoung Pharma offers both OEM and ODM services, leveraging over 20 years of experience in international transactions.
Q:What are the main markets for Reyoung Pharma's products?
A:
Products are exported to over 70 countries, covering Asia, South America, Africa, CIS Countries, the Middle East, and Europe.

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