Product NDC: | 45963-125 |
Proprietary Name: | Infants Ibuprofen |
Non Proprietary Name: | concetrated ibuprofen |
Active Ingredient(s): | 50 mg/1.25mL & nbsp; concetrated ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 45963-125 |
Labeler Name: | Actavis Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079058 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100520 |
Package NDC: | 45963-125-23 |
Package Description: | 1 BOTTLE in 1 CARTON (45963-125-23) > 15 mL in 1 BOTTLE |
NDC Code | 45963-125-23 |
Proprietary Name | Infants Ibuprofen |
Package Description | 1 BOTTLE in 1 CARTON (45963-125-23) > 15 mL in 1 BOTTLE |
Product NDC | 45963-125 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | concetrated ibuprofen |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20100520 |
Marketing Category Name | ANDA |
Labeler Name | Actavis Inc. |
Substance Name | IBUPROFEN |
Strength Number | 50 |
Strength Unit | mg/1.25mL |
Pharmaceutical Classes |