OxyContin - oxycodone hydrochloride
Navigation: NDC > Supplier starting with: P > PURDUE PHARMA LP| Field | Value |
|---|---|
| NDC Code: | 59011-410 |
| Proprietary Name: | OxyContin |
| Suffix: | |
| Non-Proprietary Name: | oxycodone hydrochloride |
| Dosage Form: | TABLET, FILM COATED, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 08-08-2010 |
| Category Name: | NDA |
| Application Number: | NDA022272 |
| Labeler: | PURDUE PHARMA LP |
| Substance Name: | OXYCODONE HYDROCHLORIDE |
| Active Numerator Strength: | 10 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: | CII |