Details for New Drug Application (NDA): 076925
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 076925
| Tradename: | IBUPROFEN |
| Applicant: | Padagis Us |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 076925
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 076925
Suppliers and Packaging for NDA: 076925
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | SUSPENSION;ORAL | 076925 | ANDA | Padagis Israel Pharmaceuticals Ltd | 45802-952 | 45802-952-26 | 1 BOTTLE in 1 CARTON (45802-952-26) / 120 mL in 1 BOTTLE |
| IBUPROFEN | ibuprofen | SUSPENSION;ORAL | 076925 | ANDA | Padagis Israel Pharmaceuticals Ltd | 45802-952 | 45802-952-43 | 473 mL in 1 BOTTLE (45802-952-43) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | SUSPENSION;ORAL | Strength | 100MG/5ML | ||||
| Approval Date: | Sep 23, 2004 | TE: | AB | RLD: | No | ||||
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