OXYCODONE HCL is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Direct Rx. The primary component is Oxycodone Hydrochloride.
| Product ID | 61919-671_2c632617-2b8b-527c-e054-00144ff8d46c |
| NDC | 61919-671 |
| Product Type | Human Prescription Drug |
| Proprietary Name | OXYCODONE HCL |
| Generic Name | Oxycodone Hcl |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 2016-02-22 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA203638 |
| Labeler Name | DIRECT RX |
| Substance Name | OXYCODONE HYDROCHLORIDE |
| Active Ingredient Strength | 30 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 | 2016-02-22 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | ANDA |
| Application Number | ANDA203638 |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Billing Unit | EA |
| Marketing Start Date | 2016-02-22 |
| Ingredient | Strength |
|---|---|
| OXYCODONE HYDROCHLORIDE | 30 mg/1 |
| SPL SET ID: | 2c632617-2b8a-527c-e054-00144ff8d46c |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 10702-801 | OXYCODONE HCl | OXYCODONE HCl |
| 10702-803 | OXYCODONE HCl | OXYCODONE HCl |
| 10702-805 | OXYCODONE HCl | OXYCODONE HCl |
| 55700-791 | OXYCODONE HCl | OXYCODONE HCl |
| 61919-659 | Oxycodone HCL | Oxycodone HCL |
| 61919-671 | OXYCODONE HCL | OXYCODONE HCL |
| 63304-683 | OXYCODONE HCl | oxycodone hydrochloride |
| 63304-684 | OXYCODONE HCl | oxycodone hydrochloride |
| 69238-2294 | Oxycodone HCl | Oxycodone HCl |
| 69238-2296 | Oxycodone HCl | Oxycodone HCl |
| 69238-2298 | Oxycodone HCl | Oxycodone HCl |
| 69238-2300 | Oxycodone HCl | Oxycodone HCl |