Xartemis XR is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Specgx Llc. The primary component is Oxycodone Hydrochloride; Acetaminophen.
Product ID | 23635-115_07db75be-c9b9-425c-9024-f908a104ecfe |
NDC | 23635-115 |
Product Type | Human Prescription Drug |
Proprietary Name | Xartemis XR |
Generic Name | Oxycodone Hydrochloride And Acetaminophen |
Dosage Form | Tablet, Coated |
Route of Administration | ORAL |
Marketing Start Date | 2013-04-30 |
Marketing End Date | 2019-05-31 |
Marketing Category | NDA / NDA |
Application Number | NDA204031 |
Labeler Name | SpecGx LLC |
Substance Name | OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN |
Active Ingredient Strength | 8 mg/1; mg/1 |
Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |
NDC Exclude Flag | N |
Marketing Start Date | 2013-04-30 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA204031 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2013-04-30 |
Marketing End Date | 2019-05-31 |
Marketing Category | NDA |
Application Number | NDA204031 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2013-04-30 |
Marketing End Date | 2019-05-31 |
Ingredient | Strength |
---|---|
OXYCODONE HYDROCHLORIDE | 7.5 mg/1 |
SPL SET ID: | efcb1e8b-c0be-47ee-b09e-7a6b41e64bdd |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
UPC Code |
NDC | Brand Name | Generic Name |
---|---|---|
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 |
63481-623 | PERCOCET | oxycodone hydrochloride and acetaminophen |
63481-627 | PERCOCET | oxycodone hydrochloride and acetaminophen |
23635-115 | Xartemis | oxycodone hydrochloride and acetaminophen |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
XARTEMIS 85705518 4632837 Live/Registered |
Mallinckrodt LLC 2012-08-16 |