High Purity Pharmaceutical API Oxytetracycline HCl Oxytetracycline Base 99% From GMP Manufacturers

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Product Description

Overview
Product Description
Certifications
Company Profile
Workshop
Packaging & Shipping
Our Team
FAQ

1 Basic Info & Overview

Model NO. Powder
Type Antiobic
Pharmacodynamic Influential Factors Repeated Medication
Storage Method Light Proof
Veterinary Reg. No. N/A
Sample Yes
Factory Certificate Yes
GMP Standards Yes
Quality Standard EP / BP
Transport Package 25kgs/Drum
Specification 99%
Trademark OEM / Private Label Available
Origin China
HS Code 2932
Production Capacity 100,000 kg/Month

2 Product Description

Oxytetracycline is formulated to treat active infections caused by Chlamydia (such as the chest infection psittacosis, the eye infection trachoma, and the genital infection urethritis) and critical infections caused by Mycoplasma organisms (such as pneumonia). Its hydrochloride variation is highly effective and widely used. Oxytetracycline hydrochloride presents as a yellow crystalline powder, is odorless and bitter; it easily absorbs moisture, darkens gradually when exposed to sunlight, and can degrade in alkaline environments.

This substance is exceptionally valuable in targeted treatments for nonspecific urethritis, Lyme disease, brucellosis, cholera, typhus, tularaemia, and infections caused by Chlamydia, Mycoplasma, and Rickettsia. Doxycycline serves as a preferred alternative to oxytetracycline for multiple indications due to its refined pharmacological attributes.

High Purity Pharmaceutical API Oxytetracycline HCl Oxytetracycline Base 99%
Technical Specifications
Specification 99% Usage Antibiotic
Raw Material Oxytetracycline HCl Species Cattle, cow, sheep, swine, camels
Dosage Form Powder Sample Available Yes
Packing 25kg/bag Delivery Time 3-5 Days
MOQ 1kg Payment Term T/T, D/P, D/A, L/C
GMP Certified Yes ISO9001 Certified Yes
FDA Approved Not COS Certified Not
API Oxytetracycline Base Detail View
API Oxytetracycline Quality Control Packaging
Comprehensive Overview of Active Pharmaceutical Ingredients

3 Professional Certifications

Our products are certified by leading global compliance authorities, ensuring unmatched safety, efficacy, and batch-to-batch consistency.

GMP Certificate validation for pharmaceutical production
ISO Quality assurance certification compliance record
Veterinary pharmaceutical international standard certification

4 Manufacturer Profile

Advanced GMP Production Headquarters and Laboratory Complex

Our partner manufacturer was established in 2002. It operates as a large-scale, GMP-certified veterinary drug enterprise, integrating comprehensive R&D, advanced production, and international sales of veterinary APIs, high-efficacy preparations, premixed feeds, and essential feed additives. Operating with a high-caliber Provincial Technical Center, the developer maintains an innovative R&D architecture dedicated to next-generation veterinary medication, supported by over 65 dedicated technical professionals.

The enterprise runs two state-of-the-art production bases, with the main headquarters base covering a vast area of 78,706 m². The manufacturing capacity spans 13 API products including Ivermectin, Eprinomectin, Tiamulin Fumarate, and Oxytetracycline Hydrochloride, alongside 12 streamlined preparation production lines covering injections, oral solutions, soluble powders, premixes, boluses, environmental sanitizers, and advanced disinfectants. Custom API solutions, over 100 own-label formulations, and expert OEM & ODM services are continuously offered to global partners.

Outstanding emphasis is placed on highly structured EHS (Environment, Health & Safety) systems, which has earned full ISO14001 and OHSAS18001 certifications. Strategic inventory and supply chain resilience allow the enterprise to guarantee a steady, uninterrupted product supply to international buyers.

A comprehensive quality control framework governs all processes, validated by ISO9001 certificates, state GMP certificates, Australian APVMA GMP clearances, Ethiopian GMP validations, Ivermectin CEP certificates, and successful US FDA inspections. A professional registration, sales, and technical support network ensures seamless international partnership, exporting to over 60 countries and regions spanning Europe, South America, the Middle East, Africa, and Asia.

EHS Standard Compliant Modern Warehousing Facility

5 Production Workshop

A look inside our ultra-clean, fully automated production environment, built and maintained strictly according to international GMP cleanroom regulations.

Advanced Cleanroom Facilities and Automated Synthesis Line

6 Packaging & Shipping Logistical Standards

Strict packaging protocols are implemented to preserve product integrity, prevent contamination, and guarantee safe, compliant international transit.

Secure packaging drums and logistics preparation for global export

7 Technical Experts & Staff

Professional Veterinary R&D, Technical Service and Quality Control Team

? Frequently Asked Questions (FAQ)

Q1: What is the scale and experience of the manufacturer?
Established in 2002, our manufacturing facility operates as a leading veterinary pharmaceuticals expert with more than two decades of dedicated production experience, supplying API and custom formulas to over 60 countries and regions with a staff of over 400 professionals.
Q2: How is the quality of APIs and pharmaceutical products guaranteed?
We utilize a strict, double-verified Quality Management System. The facilities hold full ISO 9001 certificates, GMP certifications, APVMA GMP compliance, CEP documentation, and have successfully cleared comprehensive inspections by international regulatory bodies. Every batch undergoes exhaustive lab analysis before distribution.
Q3: Which veterinary API and dosage form options can be sourced?
We supply 13 top-tier API compounds—including Ivermectin, Eprinomectin, Tiamulin Hydrogen Fumarate, Abamectin, Oxytetracycline HCl, Tilmicosin, Florfenicol, and Doxycycline Hyclate—across 12 major dosage formats (such as liquid injections, oral solutions, soluble powders, premixes, granules, boluses, and highly stable disinfectants).
Q4: What sets this manufacturer apart from other market suppliers?
Our core advantages rest in a dual-base modern GMP manufacturing footprint, a specialized R&D center backed by 65 top-tier technical professionals, a resilient supply chain structure that ensures reliable continuous product supply, and extensive international regulatory registration expertise.
Q5: What are the accepted delivery terms and payment currencies?
We accommodate flexible commercial delivery requirements including EXW, FOB, CFR, and CIF. We accept global transactions in USD, EUR, and CNY via reliable mechanisms such as T/T, D/P, D/A, and L/C.
Q6: Are customized OEM and ODM services supported?
Yes. In addition to delivering superior bulk active ingredients, we provide professional OEM and ODM contract manufacturing services, complete custom formulation development, and private label support designed for global veterinary requirements.

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