Details for New Drug Application (NDA): 079129
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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 079129
| Tradename: | IBUPROFEN |
| Applicant: | Strides Pharma |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 079129
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 079129
Suppliers and Packaging for NDA: 079129
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | TABLET;ORAL | 079129 | ANDA | CVS Pharmacy | 51316-187 | 51316-187-00 | 500 TABLET in 1 BOTTLE (51316-187-00) |
| IBUPROFEN | ibuprofen | TABLET;ORAL | 079129 | ANDA | Family Dollar (FAMILY WELLNESS) | 55319-136 | 55319-136-05 | 500 TABLET, COATED in 1 BOTTLE, PLASTIC (55319-136-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
| Approval Date: | Mar 28, 2011 | TE: | RLD: | No | |||||
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