Details for New Drug Application (NDA): 077338
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The generic ingredient in IBUPROFEN is ibuprofen sodium. There are sixty-four drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the ibuprofen sodium profile page.
Summary for 077338
Tradename: | IBUPROFEN |
Applicant: | P And L Dev Llc |
Ingredient: | ibuprofen |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 077338
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | CAPSULE;ORAL | Strength | EQ 200MG FREE ACID AND POTASSIUM SALT | ||||
Approval Date: | Jul 10, 2009 | TE: | RLD: | No |
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