Oxycodone Hydrochloride
- Product NDC
- 51407-533
- 11-digit product format
- 514070533
- Labeler code
- 51407
- Product ID
- 51407-533_990e2460-85e5-7ab4-e053-2a95a90a59db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA204021
- Marketing category
- ANDA
- Marketing start
- 2017-06-12
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 30 mg/1
- Pharmacologic classes
- Full Opioid Agonists [MoA],Opioid Agonist [EPC]
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 51407-533-01 | 51407053301 | 100 TABLET in 1 BOTTLE (51407-533-01) | 100 tablet | 2019-11-26 | 0000-00-00 | No | No | Current |