NDC Code | 60760-049-90 |
Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60760-049-90) |
Product NDC | 60760-049 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Oxycontin |
Non-Proprietary Name | Oxycodone Hydrochloride |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20101230 |
Marketing Category Name | NDA |
Application Number | NDA020553 |
Manufacturer | St Marys Medical Park Pharmacy |
Substance Name | OXYCODONE HYDROCHLORIDE |
Strength | 20 |
Strength Unit | mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |