Oxycodone Hydrochloride - Oxycodone Hydrochloride
Navigation: NDC > Supplier starting with: Q > QUALITEST PHARMACEUTICALS| Field | Value |
|---|---|
| NDC Code: | 0603-4992 |
| Proprietary Name: | Oxycodone Hydrochloride |
| Suffix: | |
| Non-Proprietary Name: | Oxycodone Hydrochloride |
| Dosage Form: | TABLET |
| Method: | ORAL |
| Original Marketing Date: | 31-01-2007 |
| Category Name: | ANDA |
| Application Number: | ANDA077712 |
| Labeler: | QUALITEST PHARMACEUTICALS |
| Substance Name: | OXYCODONE HYDROCHLORIDE |
| Active Numerator Strength: | 30 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: | CII |