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Opana ER
Opana ER - 63629-4174-1 - (OXYMORPHONE HYDROCHLORIDE)
Drug Information of Opana ER
| Product NDC: | 63629-4174 |
| Proprietary Name: | Opana ER |
| Non Proprietary Name: | OXYMORPHONE HYDROCHLORIDE |
| Active Ingredient(s): | 20 mg/1 & nbsp; OXYMORPHONE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Opana ER
| Product NDC: | 63629-4174 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021610 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101231 |
Package Information of Opana ER
| Package NDC: | 63629-4174-1 |
| Package Description: | 60 TABLET in 1 BOTTLE (63629-4174-1) |
NDC Information of Opana ER
| NDC Code | 63629-4174-1 |
| Proprietary Name | Opana ER |
| Package Description | 60 TABLET in 1 BOTTLE (63629-4174-1) |
| Product NDC | 63629-4174 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | OXYMORPHONE HYDROCHLORIDE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101231 |
| Marketing Category Name | NDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | OXYMORPHONE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
