PERCOCET is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Endo Pharmaceuticals Inc.. The primary component is Oxycodone Hydrochloride; Acetaminophen.
| Product ID | 63481-629_8a04ce2f-d576-469f-91bc-5ed75e27e47e | 
| NDC | 63481-629 | 
| Product Type | Human Prescription Drug | 
| Proprietary Name | PERCOCET | 
| Generic Name | Oxycodone Hydrochloride And Acetaminophen | 
| Dosage Form | Tablet | 
| Route of Administration | ORAL | 
| Marketing Start Date | 2001-11-30 | 
| Marketing Category | ANDA / ANDA | 
| Application Number | ANDA040330 | 
| Labeler Name | Endo Pharmaceuticals Inc. | 
| Substance Name | OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN | 
| Active Ingredient Strength | 10 mg/1; mg/1 | 
| Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] | 
| DEA Schedule | CII | 
| NDC Exclude Flag | N | 
| Listing Certified Through | 2021-12-31 | 
| Marketing Start Date | 2001-11-30 | 
| NDC Exclude Flag | N | 
| Sample Package? | N | 
| Marketing Category | ANDA | 
| Application Number | ANDA040330 | 
| Product Type | HUMAN PRESCRIPTION DRUG | 
| Billing Unit | EA | 
| Marketing Start Date | 2001-11-30 | 
| Ingredient | Strength | 
|---|---|
| OXYCODONE HYDROCHLORIDE | 10 mg/1 | 
| SPL SET ID: | 4dd36cf5-8f73-404a-8b1d-3bd53bd90c25 | 
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code | 
| NDC | Brand Name | Generic Name | 
|---|---|---|
| 63481-623 | PERCOCET | oxycodone hydrochloride and acetaminophen | 
| 63481-627 | PERCOCET | oxycodone hydrochloride and acetaminophen | 
| 63481-628 | PERCOCET | PERCOCET | 
| 63481-629 | PERCOCET | PERCOCET | 
| 63629-3773 | PERCOCET | PERCOCET | 
| 63629-3776 | PERCOCET | PERCOCET | 
| 65084-298 | PERCOCET | PERCOCET | 
| 0406-0512 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen | 
| 0406-0522 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen | 
| 0406-0523 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen | 
| 0603-4978 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 0603-4979 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 0603-4982 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 0603-4998 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 0904-6437 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 0904-6438 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 0904-6439 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 10544-287 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen | 
| 21695-233 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen | 
| 21695-616 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 52959-556 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 55700-983 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen | 
| 55700-984 | OXYCODONE AND ACETAMINOPHEN | oxycodone hydrochloride and acetaminophen | 
| 63187-406 | Oxycodone and Acetaminophen | Oxycodone hydrochloride and Acetaminophen | 
| 29033-405 | Oxycodone Hydrochloride and Acetaminophen | Oxycodone Hydrochloride and Acetaminophen | 
| 46672-648 | oxycodone hydrochloride and acetaminophen | oxycodone hydrochloride and acetaminophen | 
| 60760-200 | Oxycodone Hydrochloride and Acetaminophen | Oxycodone Hydrochloride and Acetaminophen | 
| 23635-115 | Xartemis | oxycodone hydrochloride and acetaminophen | 
| Mark Image Registration | Serial | Company Trademark Application Date | 
|---|---|
|  PERCOCET  73072165  1051682 Live/Registered | ENDO LABORATORIES, INC. 1975-12-18 |