Oxycodone Hydrochloride
- Product NDC
- 0904-6591
- 11-digit product format
- 009046591
- Labeler code
- 0904
- Product ID
- 0904-6591_3b973e31-c79c-4615-9bcd-9df008928f6e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA077712
- Marketing category
- ANDA
- Marketing start
- 2007-01-31
- Marketing end
- 2021-02-28
- 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
- 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 |
|---|
| 0904-6591-61 | 00904659161 | 100 BLISTER PACK in 1 CARTON (0904-6591-61) > 1 TABLET in 1 BLISTER PACK | 100 blister pack | 2007-01-31 | 2021-02-28 | No | No | Current |