Oxycodone Hydrochloride
- Product NDC
- 68308-020
- 11-digit product format
- 683080020
- Labeler code
- 68308
- Product ID
- 68308-020_a224ae98-a97d-4033-9e9e-44e77a103316
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA204092
- Marketing category
- ANDA
- Marketing start
- 2014-06-12
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 100 mg/5mL
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68308-020-03 | 68308002003 | 1 BOTTLE, PLASTIC in 1 CARTON (68308-020-03) > 30 mL in 1 BOTTLE, PLASTIC | 2014-06-12 | 0000-00-00 | No | No | Current |