Details for New Drug Application (NDA): 213506
The generic ingredient in IBUPROFEN is ibuprofen sodium. There are eight 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 | |||||
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