Product NDC: | 50580-100 |
Proprietary Name: | Infants Motrin |
Non Proprietary Name: | Ibuprofen |
Active Ingredient(s): | 50 mg/1.25mL & nbsp; Ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION/ DROPS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50580-100 |
Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA020603 |
Marketing Category: | NDA |
Start Marketing Date: | 20040601 |
Package NDC: | 50580-100-18 |
Package Description: | 1 BOTTLE in 1 CARTON (50580-100-18) > 15 mL in 1 BOTTLE |
NDC Code | 50580-100-18 |
Proprietary Name | Infants Motrin |
Package Description | 1 BOTTLE in 1 CARTON (50580-100-18) > 15 mL in 1 BOTTLE |
Product NDC | 50580-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | SUSPENSION/ DROPS |
Route Name | ORAL |
Start Marketing Date | 20040601 |
Marketing Category Name | NDA |
Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
Substance Name | IBUPROFEN |
Strength Number | 50 |
Strength Unit | mg/1.25mL |
Pharmaceutical Classes |