Custom Manufacturing, Project Outsourcing, your Trusted Partner from China
The formulation of pharmaceutical products demands the highest standards of precision and purity, especially when it comes to Active Pharmaceutical Ingredients (APIs). Acetaminophen, a cornerstone medication for pain and fever management, must consistently meet USP (United States Pharmacopeia) and BP (British Pharmacopoeia) standards to ensure the safety and efficacy of the final drug product. NINGBO INNO PHARMCHEM CO.,LTD. is a leading provider of Acetaminophen powder that adheres to these critical pharmacopoeial requirements.
Meeting USP/BP standards for acetaminophen means rigorous testing for purity, identification, assay, and impurity profiles. These standards guarantee that the API is free from contaminants that could lead to adverse drug reactions or reduce therapeutic effectiveness. For pharmaceutical manufacturers, using acetaminophen that complies with these benchmarks is non-negotiable. It underpins the reliability of their formulations and ensures compliance with regulatory bodies worldwide. Whether producing generic pain relievers or more complex combination therapies, the foundational quality of the acetaminophen is paramount.
NINGBO INNO PHARMCHEM CO.,LTD. is committed to upholding these rigorous standards. We understand that our clients rely on us for a consistent supply of USP/BP standard acetaminophen powder to meet their manufacturing needs. This commitment extends from our manufacturing processes to our documentation, providing our partners with the necessary assurances for regulatory submission and market approval. The availability of high-purity acetaminophen powder facilitates the development of safe and effective medications that improve patient outcomes.
By choosing NINGBO INNO PHARMCHEM CO.,LTD. as your supplier, you ensure that your drug formulations are built upon a foundation of quality and compliance. Our dedication to providing USP/BP standard acetaminophen powder reflects our understanding of the pharmaceutical industry's demands and our commitment to supporting advancements in healthcare. Partner with us to source this essential API and ensure the integrity and success of your pharmaceutical products.
Manufacturing Facilities
Professional Export Experience
to Global Customers
1. 20 years of R&D, manufacturing and sales experience, serving customers in 60 countries and regions around the world;
2. Own R&D laboratory, pilot platform and large-scale production workshop, which can meet the audit requirements of global customers;
3. We can satisfy customers' perfect transition from small scale lab requirements (gram level) to commercialization requirements (hundred tons level).
A: We don't have Minimum Order Quantity, exact quantity should be provided before quotation for us to calculate the exact cost.
A: We don't provide free samples due to lots of request and expensive international courier's cost, we can deduct the sample charge after commercial order placed.
A: Our payment terms: Small or sample order: T/T IN ADVANCE. Commercial order: First order should be by T/T IN ADVANCE or L/C at sight, and following orders T/T 30~90days is acceptable subject to approval of credit application.
