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IBU
IBU - 50436-4604-0 - (Ibuprofen)
Drug Information of IBU
| Product NDC: | 50436-4604 |
| Proprietary Name: | IBU |
| Non Proprietary Name: | Ibuprofen |
| Active Ingredient(s): | 400 mg/1 & nbsp; Ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of IBU
| Product NDC: | 50436-4604 |
| Labeler Name: | Unit Dose Services |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075682 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081120 |
Package Information of IBU
| Package NDC: | 50436-4604-0 |
| Package Description: | 12 TABLET in 1 BOTTLE (50436-4604-0) |
NDC Information of IBU
| NDC Code | 50436-4604-0 |
| Proprietary Name | IBU |
| Package Description | 12 TABLET in 1 BOTTLE (50436-4604-0) |
| Product NDC | 50436-4604 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ibuprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081120 |
| Marketing Category Name | ANDA |
| Labeler Name | Unit Dose Services |
| Substance Name | IBUPROFEN |
| Strength Number | 400 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
