oxycodone hydrochloride - oxycodone hydrochloride
Navigation: NDC > Supplier starting with: E > ETHEX CORPORATION| Field | Value |
|---|---|
| NDC Code: | 58177-679 |
| Proprietary Name: | oxycodone hydrochloride |
| Suffix: | controlled-release |
| Non-Proprietary Name: | oxycodone hydrochloride |
| Dosage Form: | TABLET, EXTENDED RELEASE |
| Method: | ORAL |
| Original Marketing Date: | 25-09-2009 |
| Category Name: | NDA AUTHORIZED GENERIC |
| Application Number: | NDA020553 |
| Labeler: | ETHEX CORPORATION |
| Substance Name: | OXYCODONE HYDROCHLORIDE |
| Active Numerator Strength: | 20 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: | CII |