Product NDC: | 54569-4002 |
Proprietary Name: | Ibuprofen |
Non Proprietary Name: | Ibuprofen |
Active Ingredient(s): | 600 mg/1 & nbsp; Ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54569-4002 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078558 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091123 |
Package NDC: | 54569-4002-2 |
Package Description: | 4 TABLET in 1 BOTTLE (54569-4002-2) |
NDC Code | 54569-4002-2 |
Proprietary Name | Ibuprofen |
Package Description | 4 TABLET in 1 BOTTLE (54569-4002-2) |
Product NDC | 54569-4002 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091123 |
Marketing Category Name | ANDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | IBUPROFEN |
Strength Number | 600 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |