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Fast-Acting 40mg Omeprazole Powder for Injection - Relief Solution
US$0.29
100,000-999,999 Pieces
US$0.19
1,000,000+ Pieces
Sample price:US$0.00/piece.Request sample

Product profile

Customization

Available

Application

Injection

Usage Mode

Injection

Model NO.

AMC13025-04

Suitable for

Doctor

State

Injection

Shape

Powder

Pharmaceutical Technology

Chemical Synthesis

Transport Package

10vials Per Box

Specification

40mg

Trademark

Medipharm, OEM

Origin

China

HS Code

3004909099

Production Capacity

75000vials/Batch

Key features

Fast-Acting Formula: Specifically inhibits H+, K+-ATPase to effectively suppress stomach acid secretion.
40mg Dosage Strength: Standardized 40mg omeprazole powder for injection with 10ml special solvent.
Versatile Clinical Applications: Treats peptic ulcer hemorrhage, acute gastric mucosal injury, and prevents aspiration pneumonia.
ISO Certified Manufacturing: Manufactured under ISO45001:2018 and ISO14001 certified management systems.
Full Customization Available: Offers customization from designs, samples, and full customization services.
Global Market Reach: Exports to South America, Southeast Asia, Middle East, Africa, and South Asia.
Experienced Exporter: 14 years of export experience with 14 foreign trading staff and 12 supply chain partners.
Flexible Payment Terms: Accepts T/T, LC, and D/P payment methods with FOB, CIF, and EXW shipping terms.

Company profile

Anhui Medipharm Co., Ltd.
Years of Export ExperienceHigh Repeat Buyers ChoiceImporters and ExportersManagement Certification
Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 14 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤2.94h

AI-Powered supplier vetting

SummaryAnhui Medipharm Co., Ltd. is a China-based trading company established in 2010 with 32 employees and a broad healthcare-related product scope. It has overseas agents or branches, participated in the 136th Canton Fair, and exports 90% of total sales, but no overseas showroom is reported. Service procedures, corrective and preventive action procedures, and complaint-handling procedures are documented and supported by records. The supplier reports ISO9001:2015, ISO45001:2018, and ISO14001 certifications, although it lacks a factory environmental impact assessment report. Innovation and customization are supported by recent new products, ODM services, and multiple customization methods. Production capability is not demonstrated because the supplier is identified as a trading company and no manufacturing capacity is provided. Financial information only identifies reporting years, without substantive performance data. No specific customer cases are provided.
Supplier typeThe supplier is identified as a trading company or trade company, organized as a limited company in Hefei, Anhui, China, with 32 employees. Its listed product scope covers medicines, veterinary drugs, nutritional and medical products, additives, APIs, and related categories, indicating broad trading coverage rather than confirmed in-house manufacturing.
CertificationsThe supplier reports ISO9001:2015, ISO45001:2018, and ISO14001 certifications. However, it also reports no factory environmental impact assessment report; this does not negate the stated certifications but indicates incomplete environmental documentation for factory-related assessment.
After-Sales capabilityThe supplier has overseas agents or branches, has participated in the 136th Canton Fair, and serves listed markets including Papua New Guinea and Cameroon. Written procedures and records exist for service assessment, corrective and preventive actions, and customer complaints, while stated peak- and off-season lead times are both one month.
R&D capabilityThe supplier reports launching new products during the past year and provides ODM services, supporting active product development. It does not provide an SDK and does not offer OEM services for well-known brands, so the evidence supports product innovation but not software-development or major-brand OEM capability.
Customization capabilityThe supplier reports customization from designs, customization from samples, and full customization, as well as ODM service availability. These statements explicitly support a broad customization offering, although the evidence does not quantify capacity or specify production ownership.

Product Q&A

Q:What are the main clinical applications of this product?
A:
It is used for peptic ulcer hemorrhage, anastomotic ulcer hemorrhage, acute gastric mucosal injury, and prevention of acid reflux combined with aspiration pneumonia in patients under general anesthesia.
Q:How should the product be administered?
A:
It is administered via intravenous injection. One 40mg bottle is dissolved with 10ml of special solvent and must be used within 2 hours after dissolving.
Q:Is this product suitable for pregnant women?
A:
Although animal experiments have not shown adverse effects, it is suggested that pregnant and lactating women avoid using this product if possible.
Q:What is the recommended dosage for adults?
A:
The standard dosage is one 40mg dose, administered 1 to 2 times per day.
Q:Are there any drug interactions to be aware of?
A:
Yes, it may interact with phenytoin sodium and drugs metabolized by the cytochrome P450 enzyme system like warfarin. Close monitoring is required.

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