Advil is a Oral Tablet, Coated in the Human Otc Drug category. It is labeled and distributed by Glaxosmithkline Consumer Healthcare Holdings (us) Llc. The primary component is Ibuprofen Sodium.
Product ID | 0573-0133_4e46a19d-ca33-44b9-bf35-a1da6a4be764 |
NDC | 0573-0133 |
Product Type | Human Otc Drug |
Proprietary Name | Advil |
Generic Name | Ibuprofen Sodium |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA / NDA |
Application Number | NDA201803 |
Labeler Name | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
Substance Name | IBUPROFEN SODIUM |
Active Ingredient Strength | 256 mg/1 |
Pharm Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
NDC Exclude Flag | N |
Listing Certified Through | 2023-12-31 |
Marketing Start Date | 2014-08-11 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2015-08-12 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-12-01 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2014-08-11 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-07-08 |
Marketing Category | NDA |
Application Number | NDA201803 |
Product Type | HUMAN OTC DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-07-08 |
Ingredient | Strength |
---|---|
IBUPROFEN SODIUM | 256 mg/1 |
SPL SET ID: | 5be198b8-396e-4b44-8819-e2e3b5d2ad0e |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0573-0133 | Advil | ibuprofen sodium |
0573-0134 | Advil | ibuprofen sodium |
0573-0149 | Advil | ibuprofen |
0573-0150 | ADVIL | ibuprofen |
0573-0151 | ADVIL | ibuprofen |
0573-0154 | ADVIL | ibuprofen |
0573-0160 | ADVIL | ibuprofen |
0573-0161 | ADVIL | ibuprofen |
0573-0165 | ADVIL | ibuprofen |
67751-146 | Advil | Advil |
0573-0169 | Advil | Advil |
0573-0166 | ADVIL | ADVIL |
0573-1769 | Advil | Advil |
0573-1711 | ADVIL | ADVIL |
66715-9700 | Advil | Advil |
52904-790 | ADVIL | ADVIL |
52904-786 | ADVIL | ADVIL |
52904-794 | ADVIL | ADVIL |
52904-791 | ADVIL | ADVIL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ADVIL 98830145 not registered Live/Pending |
Haleon US IP LLC 2024-10-31 |
ADVIL 98106239 not registered Live/Pending |
GlaxoSmithKline Consumer Healthcare (US) IP LLC 2023-07-28 |
ADVIL 78944373 not registered Dead/Abandoned |
Wyeth 2006-08-03 |
ADVIL 78144235 not registered Dead/Abandoned |
Wyeth 2002-07-16 |
ADVIL 74622037 1942746 Live/Registered |
PF CONSUMER HEALTHCARE 1 LLC 1995-01-17 |
ADVIL 74048209 1635943 Live/Registered |
Boots Company PLC, The 1990-04-11 |
ADVIL 73435737 1298347 Live/Registered |
Boots Company PLC, The 1983-07-22 |