Oxycodone Hydrochloride
- Product NDC
- 0904-6701
- 11-digit product format
- 009046701
- Labeler code
- 0904
- Product ID
- 0904-6701_9c234e49-d0bd-4122-b6c1-d2d2eaa4bb41
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxycodone Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA209897
- Marketing category
- ANDA
- Marketing start
- 2018-02-12
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record