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oxycodone hydrochloride and ibuprofen
oxycodone hydrochloride and ibuprofen - 0591-3494-05 - (oxycodone hydrochloride and ibuprofen)
Drug Information of oxycodone hydrochloride and ibuprofen
| Product NDC: | 0591-3494 |
| Proprietary Name: | oxycodone hydrochloride and ibuprofen |
| Non Proprietary Name: | oxycodone hydrochloride and ibuprofen |
| Active Ingredient(s): | 400; 5 mg/1; mg/1 & nbsp; oxycodone hydrochloride and ibuprofen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of oxycodone hydrochloride and ibuprofen
| Product NDC: | 0591-3494 |
| Labeler Name: | Watson Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078394 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071201 |
Package Information of oxycodone hydrochloride and ibuprofen
| Package NDC: | 0591-3494-05 |
| Package Description: | 500 TABLET in 1 BOTTLE, PLASTIC (0591-3494-05) |
NDC Information of oxycodone hydrochloride and ibuprofen
| NDC Code | 0591-3494-05 |
| Proprietary Name | oxycodone hydrochloride and ibuprofen |
| Package Description | 500 TABLET in 1 BOTTLE, PLASTIC (0591-3494-05) |
| Product NDC | 0591-3494 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxycodone hydrochloride and ibuprofen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071201 |
| Marketing Category Name | ANDA |
| Labeler Name | Watson Laboratories, Inc. |
| Substance Name | IBUPROFEN; OXYCODONE HYDROCHLORIDE |
| Strength Number | 400; 5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
