Details for New Drug Application (NDA): 075010
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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 075010
Tradename: | IBUPROFEN |
Applicant: | Lnk |
Ingredient: | ibuprofen |
Patents: | 0 |
Formulation / Manufacturing: | see details |
Pharmacology for NDA: 075010
Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 075010
Suppliers and Packaging for NDA: 075010
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
IBUPROFEN | ibuprofen | TABLET;ORAL | 075010 | ANDA | Walgreen Company | 0363-0291 | 0363-0291-03 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-03) |
IBUPROFEN | ibuprofen | TABLET;ORAL | 075010 | ANDA | Walgreen Company | 0363-0291 | 0363-0291-14 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-0291-14) |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
Approval Date: | Mar 1, 1999 | TE: | RLD: | No |
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