Details for New Drug Application (NDA): 090796
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The generic ingredient in IBUPROFEN is ibuprofen sodium. There are eight 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 090796
| Tradename: | IBUPROFEN |
| Applicant: | Marksans Pharma |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 090796
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 090796
Suppliers and Packaging for NDA: 090796
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | TABLET;ORAL | 090796 | ANDA | MARKSANS PHARMA LIMITED | 25000-121 | 25000-121-03 | 30 TABLET in 1 BOTTLE (25000-121-03) |
| IBUPROFEN | ibuprofen | TABLET;ORAL | 090796 | ANDA | MARKSANS PHARMA LIMITED | 25000-121 | 25000-121-12 | 500 TABLET in 1 BOTTLE (25000-121-12) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 400MG | ||||
| Approval Date: | Dec 21, 2010 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 600MG | ||||
| Approval Date: | Dec 21, 2010 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 800MG | ||||
| Approval Date: | Dec 21, 2010 | TE: | AB | RLD: | No | ||||
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