Oxycodone Hydrochloride - Oxycodone Hydrochloride
Navigation: NDC > Supplier starting with: Z > ZYDUS PHARMACEUTICALS (USA) INC.| Field | Value |
|---|---|
| NDC Code: | 68382-796 |
| Proprietary Name: | Oxycodone Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Oxycodone Hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 26-12-2012 |
| Category Name: | ANDA |
| Application Number: | ANDA077290 |
| Labeler: | ZYDUS PHARMACEUTICALS (USA) INC. |
| 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 |