Tang's Pharma Chemical Co., Ltd. >> Paracetamol Acetaminophen ( Tablet & Raw Materical )

Paracetamol Acetaminophen ( Tablet & Raw Materical )

Paracetamol Acetaminophen ( Tablet & Raw Materical )
Price: Negotiable
Min Order: 1
We export Active Pharmaceutical Ingredient ( API) and tablet ( 500mg &325mg ) to Africa and some Europe countries, Paracetamol manufactured by us with the syrup of strawberry taste is very popular in Africa. We accept the OEM co-operation for all kinds of Cream, Capsules, Tablets. Details please contract with us.
For Paracetamol regulatory status:
-Facility and process engineering Designed under strictiest international cGMP standards
-hold certification of Suitability granted by EDQM
-filed US DMF
-registered in overseas markets
High-pressure reaction autoclave

1. Lab scale: 100ml, 500ml, 1000ml, 2000ml two sets each
Highest Pressure: 12MPa
2. Pilot scale: 50L(one set, 12.5Mpa), 100L(one set, 1.59Mpa), 500L( fours sets, 1.59Mpa and 11Mpa)
Highest Pressure: 12MPa
3. Production scale: 1500L(four sets, 6Mpa), 2000L( six sets, 1.59Mpa), 3000L(two sets, 1.59Mpa), 1000L( 10 sets, )
Highest pressure: 6Mpa

Quality Assurance:
TANG'S pursues high purity and consistently reliable quality by stringent quality control and processes management.
· Each production process has a proper quality standard, test and analysis methods
· All of associates plants obtained ISO9000 certificate
· Following analysis methods for our product testing:
Gas chromatography (GC),
Thin Layer Chromatography (TLC),
Nuclear Magnetic Resonance (NMR),
Elementary Analysis.

After Sales Service:
The clients can get safe and efficient service from our professional sales.
· Strictly keep secret with commercial and technical agreements signed with clients.
· Prompt response to clients' requirements and inquiries, effective resolution for client complaints.
· Registrations support for overseas sales of regular clients.
· Delivery on time, packaging with labels and marks as per client instructions.
· Standard documents: Commercial Invoice, Packing List, Certificate of Analysis (COA), Material Safety Data Sheet (MSDS), Form A, Certificate of Origin and Bill of Lading (B/L), etc.
· Cooperation with clients in the compilation of Drug Master Files (DMF) of APIs for regulatory compliance; Related audit on Documentation, technical and on-site etc.

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