High Quality Aspirin DC, Ciprofloxacin DC, Naproxen DC

Product Details
Customization: Available
Function: Antipyretic Analgesic and Non-Steroidal Anti-Inflammatory Analgesic
Certification: GMP, Reach
Gold Member Since 2005

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Management System Certification
ISO 9001, ISO 14000, ISO 20000, GMP, HACCP
Terms of Payment
LC, T/T, Western Union
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Basic Info.

Model NO.
IBP
Type
Chemical Reagent
State
Solid
Volatile
Not Volatile
OEM
Available
Sample
Available
Form
Powder
Color
White
Transport Package
25kgs/Drum
Specification
GMP, USP/BP
Trademark
Fraken
Origin
China
Production Capacity
10, 000mt Per Year

Product Description

Ibuprofen
CAS15687-27-1
MF: C13H18O2
EINECS: 239-784-6
Standard: USP/BP
Content: 99%

UsageIbuprofen is a nonsteroidal anti-inflammatory drug (NSAID) used for relief of symptoms of arthritis, fever, as an analgesic (pain reliever), especially where there is an inflammatory component, and dysmenorrhea.


ApplicationIbuprofen is used primarily for fever, pain, dysmenorrhea and inflammatory diseases such as rheumatoid arthritis. It is also used for pericarditis and patent ductus arteriosus.

Ibuprofen DC
Content: DC65/DC65/ DC68/DC73/DC85/DC90
Packing: 25kgs/drum

It is white granule, used for pressing tablet of Ibuprofen tablets.


Ibuprofen Lysine / Ibuprofen Lysinate
It is a nonsteroidal anti-inflammatory drug (NSAID). It is used to close a heart defect called patent ductus arteriosus (PDA) in a baby who was born early.


Aspirin DC
Content: DC90/DC100
Packing: 25kgs/drum

Ciprofloxacin DC
Content: DC65
Packing: 25kgs/drum

Naproxen DC
Content: DC80
Packing: 25kgs/drum

Name Active ingredient Grade & assay of Active ingredient
Naproxen Sodium DC Naproxen Sodium DC 90 88.0%-92.0%
DC 97 95.0%-99.0%
DC 98 96.0%-99.0%
ITEMS
 
SPECIFICATIONS
 
RESULTS
 
Appearance 
 
White, crystalline powder or colorless crystals
 
Passes
 
Identification
 
Accord With BP2007
 
Passes
 
Assay
 
98.5%~101.0%
 
99.97%
 
Melting point
 
75°C~78°C
 
77°C
 
Optical rotation
 
-0.05°~+0.05°
 
0.00°
 
Heavy metals
 
≤ 0.001%
 
<0.001%
 
Related substances 
 
Impurity B
 
≤ 0.3%
 
Passes
 
Any other impurity
 
≤ 0.3%
 
Passes
 
Total of all impurities apart from impurity B
 
≤ 0.7%
 
Passes
 
Impurity F
 
≤ 0.1%
 
Not detected
 
Sulphated ash
 
≤ 0.1%
 
0.02%
 
Appearance of solution
 
Accord With BP2007
 
Passes
 
Conclusion: COMPLY WITH BP2007
 

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