Details for New Drug Application (NDA): 211666
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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 211666
| Tradename: | IBUPROFEN |
| Applicant: | Strides Pharma |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 211666
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 211666
Suppliers and Packaging for NDA: 211666
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | SUSPENSION;ORAL | 211666 | ANDA | A-S Medication Solutions | 50090-7653 | 50090-7653-0 | 1 BOTTLE, PLASTIC in 1 CARTON (50090-7653-0) / 120 mL in 1 BOTTLE, PLASTIC |
| IBUPROFEN | ibuprofen | SUSPENSION;ORAL | 211666 | ANDA | TARO PHARMACEUTICALS U.S.A., INC. | 51672-5321 | 51672-5321-1 | 1 BOTTLE, PLASTIC in 1 CARTON (51672-5321-1) / 240 mL in 1 BOTTLE, PLASTIC |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | SUSPENSION;ORAL | Strength | 100MG/5ML | ||||
| Approval Date: | Feb 22, 2021 | TE: | RLD: | No | |||||
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