Details for New Drug Application (NDA): 215777
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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 215777
| Tradename: | IBUPROFEN |
| Applicant: | Aurobindo Pharma Ltd |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 215777
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 215777
Suppliers and Packaging for NDA: 215777
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | CAPSULE;ORAL | 215777 | ANDA | Aurohealth LLC | 58602-858 | 58602-858-12 | 1 BOTTLE in 1 CARTON (58602-858-12) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| IBUPROFEN | ibuprofen | CAPSULE;ORAL | 215777 | ANDA | Aurohealth LLC | 58602-858 | 58602-858-18 | 1 BOTTLE in 1 CARTON (58602-858-18) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | CAPSULE;ORAL | Strength | EQ 200MG FREE ACID AND POTASSIUM SALT | ||||
| Approval Date: | Sep 14, 2023 | TE: | RLD: | No | |||||
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