Details for New Drug Application (NDA): 020402
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NDA 020402 describes ADVIL MIGRAINE LIQUI-GELS, which is a drug marketed by Haleon Us Holdings and is included in one NDA. It is available from four suppliers. Additional details are available on the ADVIL MIGRAINE LIQUI-GELS profile page.
The generic ingredient in ADVIL MIGRAINE LIQUI-GELS is ibuprofen. There are sixty-four drug master file entries for this compound. Two hundred and thirty-four suppliers are listed for this compound. Additional details are available on the ibuprofen profile page.
The generic ingredient in ADVIL MIGRAINE LIQUI-GELS is ibuprofen. There are sixty-four drug master file entries for this compound. Two hundred and thirty-four suppliers are listed for this compound. Additional details are available on the ibuprofen profile page.
Summary for 020402
| Tradename: | ADVIL MIGRAINE LIQUI-GELS |
| Applicant: | Haleon Us Holdings |
| Ingredient: | ibuprofen |
| Patents: | 0 |
| Formulation / Manufacturing: | see details |
Pharmacology for NDA: 020402
| Mechanism of Action | Cyclooxygenase Inhibitors |
Medical Subject Heading (MeSH) Categories for 020402
Suppliers and Packaging for NDA: 020402
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| ADVIL LIQUI-GELS | ibuprofen | CAPSULE;ORAL | 020402 | NDA | Haleon US Holdings LLC | 0573-0149 | 0573-0149-04 | 2 PACKET in 1 BLISTER PACK (0573-0149-04) / 2 CAPSULE, LIQUID FILLED in 1 PACKET |
| ADVIL LIQUI-GELS | ibuprofen | CAPSULE;ORAL | 020402 | NDA | Haleon US Holdings LLC | 0573-0149 | 0573-0149-13 | 1 BOTTLE in 1 CARTON (0573-0149-13) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE |
Profile for product number 001
| Active Rx/OTC/Discontinued: | OTC | Dosage: | CAPSULE;ORAL | Strength | EQ 200MG FREE ACID AND POTASSIUM SALT | ||||
| Approval Date: | Apr 20, 1995 | TE: | RLD: | Yes | |||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | OTC | Dosage: | CAPSULE;ORAL | Strength | EQ 200MG FREE ACID AND POTASSIUM SALT | ||||
| Approval Date: | Mar 16, 2000 | TE: | RLD: | Yes | |||||
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