Virtual Booth
Contact Supplier
An Enquiry
Applicant Reset all filters
01 1SUN PHARMA CANADA
Dosage Reset all filters
01 1SUSPENSION;ORAL
Regulatory Info Reset all filters
01 1OTC
Brand Name Reset all filters
01 1IBUPROFEN
RLD Reset all filters
01 1No
RLD : No
TE Code :
IBUPROFEN
Dosage Form : SUSPENSION; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 100MG/5ML
Approval Date : 2017-06-27
Application Number : 209207
RX/OTC/DISCN : OTC
ProductWeb Link
Stock Recap#PipelineProspector
MarketPlace