Details for New Drug Application (NDA): 090796
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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 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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