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Oxycodone Hydrochloride and Ibuprofen
Oxycodone Hydrochloride and Ibuprofen - 0555-0778-02 - (Oxycodone Hydrochloride and Ibuprofen)
Drug Information of Oxycodone Hydrochloride and Ibuprofen
| Product NDC: | 0555-0778 |
| 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxycodone Hydrochloride and Ibuprofen
| Product NDC: | 0555-0778 |
| Labeler Name: | Barr Laboratories Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078316 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071204 |
Package Information of Oxycodone Hydrochloride and Ibuprofen
| Package NDC: | 0555-0778-02 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (0555-0778-02) |
NDC Information of Oxycodone Hydrochloride and Ibuprofen
| NDC Code | 0555-0778-02 |
| Proprietary Name | Oxycodone Hydrochloride and Ibuprofen |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0555-0778-02) |
| Product NDC | 0555-0778 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxycodone Hydrochloride and Ibuprofen |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20071204 |
| Marketing Category Name | ANDA |
| Labeler Name | Barr 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] |
