Details for New Drug Application (NDA): 019012
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The generic ingredient in NUPRIN is ibuprofen. There are sixty-four drug master file entries for this compound. Two hundred and forty-one suppliers are listed for this compound. Additional details are available on the ibuprofen profile page.
Summary for 019012
| Tradename: | NUPRIN |
| Applicant: | Kenvue Brands |
| Ingredient: | ibuprofen |
| Patents: | 0 |
Pharmacology for NDA: 019012
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 019012
Suppliers and Packaging for NDA: 019012
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| MOTRIN IB | ibuprofen | TABLET;ORAL | 019012 | NDA | Navajo Manufacturing Company Inc. | 67751-120 | 67751-120-01 | 1 POUCH in 1 CARTON (67751-120-01) / 2 TABLET, FILM COATED in 1 POUCH |
| MOTRIN MIGRAINE PAIN | ibuprofen | TABLET;ORAL | 019012 | NDA | Navajo Manufacturing Company Inc. | 67751-120 | 67751-120-01 | 1 POUCH in 1 CARTON (67751-120-01) / 2 TABLET, FILM COATED in 1 POUCH |
Profile for product number 001
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
| Approval Date: | May 18, 1984 | TE: | RLD: | No | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | DISCN | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
| Approval Date: | Jul 29, 1987 | TE: | RLD: | No | |||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | OTC | Dosage: | TABLET;ORAL | Strength | 200MG | ||||
| Approval Date: | Dec 17, 1990 | TE: | RLD: | Yes | |||||
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