Details for New Drug Application (NDA): 206999
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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 206999
| Tradename: | IBUPROFEN |
| Applicant: | Ascent Pharms Inc |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 206999
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 206999
Suppliers and Packaging for NDA: 206999
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| IBUPROFEN | ibuprofen | CAPSULE;ORAL | 206999 | ANDA | Rite Aid Corporation | 11822-0894 | 11822-0894-1 | 160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (11822-0894-1) |
| IBUPROFEN | ibuprofen | CAPSULE;ORAL | 206999 | ANDA | Rite Aid Corporation | 11822-0894 | 11822-0894-2 | 1 BOTTLE, PLASTIC in 1 CARTON (11822-0894-2) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | CAPSULE;ORAL | Strength | EQ 200MG FREE ACID AND POTASSIUM SALT | ||||
| Approval Date: | Dec 21, 2017 | TE: | RLD: | No | |||||
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