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Applicant Reset all filters
01 1PH HEALTH
Dosage Reset all filters
01 1TABLET;ORAL
Regulatory Info Reset all filters
01 1RX
Brand Name Reset all filters
01 1IBUPROFEN AND FAMOTIDINE
RLD Reset all filters
01 1No
RLD : No
TE Code : AB
FAMOTIDINE; IBUPROFEN
Dosage Form : TABLET; ORAL
Proprietary Name : IBUPROFEN AND FAMOTIDINE
Dosage Strength : 26.6MG;800MG
Approval Date : 2024-03-22
Application Number : 203658
RX/OTC/DISCN : RX
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