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High Quality Antibiotics/Procaine Penicillin for Injection/0.6mega; 0.8mega; 1.0mega; 3.0mega/GMP Certificate
Negotiable
20,000 vial
Product profile
Customization
AvailableApplication
Internal MedicineUsage Mode
Internal UseModel NO.
0.4mega; 0.6mega; 0.8mega; 1.0mega; 3.0megaSuitable for
Elderly, Children, AdultState
PowderShape
PowderType
Inorganic ChemicalsPharmaceutical Technology
Chemical SynthesisDrug Reg./Approval No.
H37021936Transport Package
1vial/Box, 10vias/Box, 50vials/BoxSpecification
50*38*36 CMTrademark
ReyoungOrigin
ChinaProduction Capacity
2, 000, 000, 000 Per YearKey features
Broad Antibacterial Spectrum: Effective against Streptococcus, Staphylococcus, Neisseria, and anaerobic bacteria.
Multiple Dosage Options: Available in 0.6mega, 0.8mega, 1.0mega, and 3.0mega specifications.
Global GMP Compliance: Certified with Chinese GMP, PIC/S, and audits from Ethiopia, Uganda, Kenya, etc.
Established Manufacturer: Reyoung Pharma established in 1966 with 3 factory sites and 1 million sqm area.
International Market Reach: Products exported to over 70 countries and NGOs since 1997.
OEM/ODM Services: Offers customized manufacturing services with 370 R&D engineers.
Trusted Brand Credit: Rated as National Trustworthy Company and Grade AAA Credit Company.
Comprehensive Product Line: Specializes in injections, tablets, capsules, granules, and APIs.
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 dosage specifications are available?
A:
The product is available in 0.6mega, 0.8mega, 1.0mega, and 3.0mega specifications.
Q:Which certifications does the manufacturer hold?
A:
Reyoung Pharma holds Chinese GMP, PIC/S GMP, and has passed audits in Ethiopia, Uganda, Kenya, Pakistan, and other regions.
Q:What are the payment terms?
A:
Accepted payment terms include LC (Letter of Credit), T/T (Telegraphic Transfer), and D/P (Documents against Payment).
Q:What is the lead time for production?
A:
The average lead time is 1-3 months for both peak season and off-season.
Q:Does the company offer OEM or ODM services?
A:
Yes, the company provides both OEM and ODM services supported by 370 R&D engineers.
Send Inquiry
*To:
Reyoung Pharmaceutical Co., Ltd.
Reyoung Pharmaceutical Co., Ltd.*Content:
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