Details for New Drug Application (NDA): 076359
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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.
Pharmacology for NDA: 076359
Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 076359
Suppliers and Packaging for NDA: 076359
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
IBUPROFEN | ibuprofen | TABLET, CHEWABLE;ORAL | 076359 | ANDA | L. Perrigo Company | 0113-2461 | 0113-2461-62 | 1 BOTTLE in 1 CARTON (0113-2461-62) / 24 TABLET, CHEWABLE in 1 BOTTLE |
IBUPROFEN | ibuprofen | TABLET, CHEWABLE;ORAL | 076359 | ANDA | Walgreen Company | 0363-1461 | 0363-1461-62 | 1 BOTTLE in 1 CARTON (0363-1461-62) / 24 TABLET, CHEWABLE in 1 BOTTLE |
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET, CHEWABLE;ORAL | Strength | 50MG | ||||
Approval Date: | Jan 16, 2004 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET, CHEWABLE;ORAL | Strength | 100MG | ||||
Approval Date: | Jan 16, 2004 | TE: | RLD: | No |
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