Product NDC: | 0113-0057 |
Proprietary Name: | Good Sense ibuprofen |
Non Proprietary Name: | ibuprofen |
Active Ingredient(s): | 50 mg/1.25mL & nbsp; ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0113-0057 |
Labeler Name: | L Perrigo Company |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA075217 |
Marketing Category: | ANDA |
Start Marketing Date: | 20000208 |
Package NDC: | 0113-0057-05 |
Package Description: | 1 BOTTLE in 1 CARTON (0113-0057-05) > 15 mL in 1 BOTTLE |
NDC Code | 0113-0057-05 |
Proprietary Name | Good Sense ibuprofen |
Package Description | 1 BOTTLE in 1 CARTON (0113-0057-05) > 15 mL in 1 BOTTLE |
Product NDC | 0113-0057 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ibuprofen |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20000208 |
Marketing Category Name | ANDA |
Labeler Name | L Perrigo Company |
Substance Name | IBUPROFEN |
Strength Number | 50 |
Strength Unit | mg/1.25mL |
Pharmaceutical Classes |