Oxycodone Hydrochloride
- Product NDC
- 68308-145
- 11-digit product format
- 683080145
- Labeler code
- 68308
- Product ID
- 68308-145_f1a008b9-97db-40c1-94cb-dc21097ec2c6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Mayne Pharma Inc.
- Application
- ANDA203107
- Marketing category
- ANDA
- Marketing start
- 2012-07-31
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 5 mg/1
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68308-145-01 | 68308014501 | 100 CAPSULE in 1 BOTTLE, PLASTIC (68308-145-01) | 100 capsule | 2012-07-31 | 0000-00-00 | No | No | Current |