OPANA ER is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Rebel Distributors Corp. The primary component is Oxymorphone Hydrochloride.
| Product ID | 21695-949_b639732f-8eb2-4592-aca3-86faf7e5360b |
| NDC | 21695-949 |
| Product Type | Human Prescription Drug |
| Proprietary Name | OPANA ER |
| Generic Name | Oxymorphone Hydrochloride |
| Dosage Form | Tablet, Film Coated, Extended Release |
| Route of Administration | ORAL |
| Marketing Start Date | 2006-06-22 |
| Marketing Category | NDA / NDA |
| Application Number | NDA021610 |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | OXYMORPHONE HYDROCHLORIDE |
| Active Ingredient Strength | 10 mg/1 |
| Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule | CII |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2006-06-22 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | NDA |
| Application Number | NDA021610 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Marketing Start Date | 2006-06-22 |
| Inactivation Date | 2019-09-24 |
| Ingredient | Strength |
|---|---|
| OXYMORPHONE HYDROCHLORIDE | 10 mg/1 |
| SPL SET ID: | b639732f-8eb2-4592-aca3-86faf7e5360b |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 21695-948 | OPANA ER | OPANA ER |
| 21695-949 | OPANA ER | OPANA ER |
| 35356-825 | Opana ER | Opana ER |
| 35356-848 | Opana ER | Opana ER |
| 35356-849 | Opana ER | Opana ER |
| 35356-820 | Opana ER | Opana ER |
| 63481-816 | Opana ER | Opana ER |
| 63481-817 | Opana ER | Opana ER |
| 63481-814 | Opana ER | Opana ER |
| 63481-815 | Opana ER | Opana ER |
| 63481-818 | Opana ER | Opana ER |
| 63481-812 | Opana ER | Opana ER |
| 63481-813 | Opana ER | Opana ER |
| 63629-4174 | Opana ER | Opana ER |
| 63629-4177 | OPANA ER | OPANA ER |
| 0054-0283 | Oxymorphone Hydrochloride | oxymorphone hydrochloride |
| 0054-0284 | Oxymorphone Hydrochloride | oxymorphone hydrochloride |
| 0115-1231 | Oxymorphone hydrochloride | Oxymorphone hydrochloride |
| 0115-1232 | Oxymorphone hydrochloride | Oxymorphone hydrochloride |
| 0115-1233 | Oxymorphone hydrochloride | Oxymorphone hydrochloride |
| 0115-1234 | Oxymorphone hydrochloride | Oxymorphone hydrochloride |
| 0115-1315 | Oxymorphone hydrochloride | Oxymorphone hydrochloride |
| 0115-1316 | Oxymorphone hydrochloride | Oxymorphone hydrochloride |
| 0115-1317 | Oxymorphone hydrochloride | Oxymorphone hydrochloride |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() OPANA ER 85341864 4101723 Dead/Cancelled |
Endo Pharmaceuticals Inc. 2011-06-09 |