Oxycodone and Aspirin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Mayne Pharma Inc.. The primary component is Oxycodone Hydrochloride; Aspirin.
Product ID | 68308-845_0fa56226-3a68-4951-a958-2acde03d3cdf |
NDC | 68308-845 |
Product Type | Human Prescription Drug |
Proprietary Name | Oxycodone and Aspirin |
Generic Name | Oxycodone Hydrochloride And Aspirin |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2011-05-02 |
Marketing Category | ANDA / ANDA |
Application Number | ANDA091670 |
Labeler Name | Mayne Pharma Inc. |
Substance Name | OXYCODONE HYDROCHLORIDE; ASPIRIN |
Active Ingredient Strength | 5 mg/1; mg/1 |
Pharm Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC],Platelet Aggregation Inhibitor [EPC],Decreased Platelet Aggregation [PE],Cyclooxygenase Inhibitors [MoA],Decreased Prostaglandin Production [PE],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC] |
DEA Schedule | CII |
NDC Exclude Flag | N |
Listing Certified Through | 2021-12-31 |
Marketing Start Date | 2011-05-02 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | ANDA |
Application Number | ANDA091670 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2011-05-02 |
Ingredient | Strength |
---|---|
OXYCODONE HYDROCHLORIDE | 4.8355 mg/1 |
SPL SET ID: | 3848642e-cc9e-4150-8199-281b294c18bc |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI | |
Pharm Class PE | |
PHarm Class EPC | |
UPC Code | |
NUI Code |
NDC | Brand Name | Generic Name |
---|---|---|
0591-3551 | Oxycodone and Aspirin | Oxycodone and Aspirin |
68308-845 | Oxycodone and Aspirin | Oxycodone Hydrochloride and Aspirin |