Product NDC: | 0573-0175 |
Proprietary Name: | JUNIOR STRENGTH ADVIL |
Non Proprietary Name: | ibuprofen |
Active Ingredient(s): | 100 mg/1 & nbsp; ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-0175 |
Labeler Name: | Pfizer Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020267 |
Marketing Category: | NDA |
Start Marketing Date: | 20110621 |
Package NDC: | 0573-0175-11 |
Package Description: | 1 BOTTLE in 1 CARTON (0573-0175-11) > 24 TABLET, COATED in 1 BOTTLE |
NDC Code | 0573-0175-11 |
Proprietary Name | JUNIOR STRENGTH ADVIL |
Package Description | 1 BOTTLE in 1 CARTON (0573-0175-11) > 24 TABLET, COATED in 1 BOTTLE |
Product NDC | 0573-0175 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ibuprofen |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20110621 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Consumer Healthcare |
Substance Name | IBUPROFEN |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes |