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Applicant Reset all filters
01 1SUPERPHARM
Dosage Reset all filters
01 1TABLET;ORAL
Regulatory Info Reset all filters
01 1DISCN
Brand Name Reset all filters
01 1IBUPROFEN
RLD Reset all filters
01 1No
RLD : No
TE Code :
IBUPROFEN
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN
Dosage Strength : 600MG
Approval Date : 1986-04-25
Application Number : 70709
RX/OTC/DISCN : DISCN
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