Details for New Drug Application (NDA): 206989
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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 206989
Tradename: | IBUPROFEN |
Applicant: | Strides Pharma |
Ingredient: | ibuprofen |
Patents: | 0 |
Pharmacology for NDA: 206989
Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 206989
Suppliers and Packaging for NDA: 206989
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
IBUPROFEN | ibuprofen | TABLET;ORAL | 206989 | ANDA | Strides Pharma Inc | 59556-811 | 59556-811-06 | 1 BOTTLE in 1 CARTON (59556-811-06) / 100 TABLET, COATED in 1 BOTTLE |
IBUPROFEN | ibuprofen | TABLET;ORAL | 206989 | ANDA | Strides Pharma Inc | 59556-811 | 59556-811-08 | 1 BOTTLE in 1 CARTON (59556-811-08) / 1000 TABLET, COATED in 1 BOTTLE |
Profile for product number 001
Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
Approval Date: | Jun 29, 2018 | TE: | RLD: | No |
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