OXYCODONE HYDROCHLORIDE
- Product NDC
- 50436-3182
- 11-digit product format
- 504363182
- Labeler code
- 50436
- Product ID
- 50436-3182_5d4a1e42-6371-435a-9b80-7ed997f6515a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- OXYCODONE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA077290
- Marketing category
- ANDA
- Marketing start
- 2012-12-26
- Marketing end
- 0000-00-00
- Substance
- OXYCODONE HYDROCHLORIDE
- Active strength
- 15 mg/1
- 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