Home
>
National Drug Code (NDC)
>
IBU
IBU - 49999-042-00 - (Ibuprofen)
Drug Information of IBU
| Product NDC: | 49999-042 |
| Proprietary Name: | IBU |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 800 mg/1 & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IBU
| Product NDC: | 49999-042 |
| Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076112 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101019 |
Package Information of IBU
| Package NDC: | 49999-042-00 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (49999-042-00) |
NDC Information of IBU
| NDC Code | 49999-042-00 |
| Proprietary Name | IBU |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (49999-042-00) |
| Product NDC | 49999-042 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101019 |
| Marketing Category Name | ANDA |
| Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
| Substance Name | IBUPROFEN |
| Strength Number | 800 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
