Oxymorphone hydrochloride
- Product NDC
- 55700-423
- 11-digit product format
- 557000423
- Labeler code
- 55700
- Product ID
- 55700-423_b83f929b-8d0b-4956-80c8-431c6f8d8754
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Oxymorphone hydrochloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA079087
- Marketing category
- ANDA
- Marketing start
- 2013-01-02
- Marketing end
- 0000-00-00
- Substance
- OXYMORPHONE 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