Oxycodone and Aspirin
- Product NDC
- 68308-845
- 11-digit product format
- 683080845
- Labeler code
- 68308
- Product ID
- 68308-845_ad703177-774d-4319-a52f-ffb80df2fa71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride and Aspirin
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA091670
- Marketing category
- ANDA
- Marketing start
- 2011-05-02
- Marketing end
- 2021-06-30
- Substance
- OXYCODONE HYDROCHLORIDE; ASPIRIN
- Active strength
- 5 mg/1; mg/1
- Pharmacologic 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
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68308-845-01 | 68308084501 | 100 TABLET in 1 BOTTLE, PLASTIC (68308-845-01) | 100 tablet | 2011-05-02 | 0000-00-00 | No | No | Current |