Details for New Drug Application (NDA): 213506
✉ Email this page to a colleague
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 213506
| Tradename: | IBUPROFEN |
| Applicant: | Aurobindo Pharma Ltd |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 213506
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 213506
Suppliers and Packaging for NDA: 213506
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | SUSPENSION/DROPS;ORAL | 213506 | ANDA | Aurohealth LLC | 58602-227 | 58602-227-04 | 1 BOTTLE in 1 CARTON (58602-227-04) / 15 mL in 1 BOTTLE |
| IBUPROFEN | ibuprofen | SUSPENSION/DROPS;ORAL | 213506 | ANDA | Aurohealth LLC | 58602-227 | 58602-227-07 | 1 BOTTLE in 1 CARTON (58602-227-07) / 30 mL in 1 BOTTLE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | SUSPENSION/DROPS;ORAL | Strength | 40MG/ML | ||||
| Approval Date: | Apr 8, 2024 | TE: | RLD: | No | |||||
Complete Access Available with Subscription
