Details for New Drug Application (NDA): 206999
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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 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 | TARGET Corporation | 11673-850 | 11673-850-16 | 1 BOTTLE, PLASTIC in 1 BOX (11673-850-16) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC |
IBUPROFEN | ibuprofen | CAPSULE;ORAL | 206999 | ANDA | TARGET Corporation | 11673-850 | 11673-850-30 | 300 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (11673-850-30) |
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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