Details for New Drug Application (NDA): 071335
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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 071335
| Tradename: | IBUPROFEN |
| Applicant: | Amneal Pharms Ny |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 071335
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 071335
Suppliers and Packaging for NDA: 071335
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | TABLET;ORAL | 071335 | ANDA | Amneal Pharmaceuticals of New York LLC | 53746-132 | 53746-132-01 | 100 TABLET in 1 BOTTLE (53746-132-01) |
| IBUPROFEN | ibuprofen | TABLET;ORAL | 071335 | ANDA | Amneal Pharmaceuticals of New York LLC | 53746-132 | 53746-132-05 | 500 TABLET in 1 BOTTLE (53746-132-05) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 600MG | ||||
| Approval Date: | Nov 25, 1986 | TE: | AB | RLD: | No | ||||
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