Oxycodone Hydrochloride
- Product NDC
- 48433-347
- 11-digit product format
- 484330347
- Labeler code
- 48433
- Product ID
- 48433-347_7d16ab89-5dfe-4ceb-ada3-cec47c7ea9fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Safecor Health, LLC
- Application
- NDA200535
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-09-23
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Full Opioid Agonists [MoA], Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48433-347-47 | 48433034747 | .25 mL in 1 SYRINGE (48433-347-47) | 2013-09-23 | 0000-00-00 | No | No | Current |
| 48433-347-55 | 48433034755 | .5 mL in 1 SYRINGE (48433-347-55) | 2013-09-23 | 0000-00-00 | No | No | Current |