Details for New Drug Application (NDA): 019012
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NDA 019012 describes NUPRIN, which is a drug marketed by Bristol Myers and J And J Consumer Inc and is included in three NDAs. It is available from two suppliers. Additional details are available on the NUPRIN profile page.
The generic ingredient in NUPRIN is ibuprofen. There are sixty-four drug master file entries for this compound. Two hundred and thirty-eight suppliers are listed for this compound. Additional details are available on the ibuprofen profile page.
The generic ingredient in NUPRIN is ibuprofen. There are sixty-four drug master file entries for this compound. Two hundred and thirty-eight suppliers are listed for this compound. Additional details are available on the ibuprofen profile page.
Summary for 019012
| Tradename: | NUPRIN |
| Applicant: | J And J Consumer Inc |
| 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 | Lil' Drug Store Products, Inc. | 29485-1465 | 29485-1465-4 | 2 POUCH in 1 PACKAGE (29485-1465-4) / 2 TABLET, FILM COATED in 1 POUCH |
| MOTRIN IB | ibuprofen | TABLET;ORAL | 019012 | NDA | Lil' Drug Store Products, Inc. | 29485-6512 | 29485-6512-4 | 2 POUCH in 1 CARTON (29485-6512-4) / 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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