oxycodone hydrochloride
- Product NDC
- 63629-4155
- 11-digit product format
- 636294155
- Labeler code
- 63629
- Product ID
- 63629-4155_4f92eca1-edf5-4b22-a66e-69c549dda71f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxycodone hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- bryant ranch prepack
- Application
- ANDA077712
- Marketing category
- ANDA
- Marketing start
- 2010-03-08
- 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
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record