NDC Code | 69238-2296-1 |
Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2296-1) |
Product NDC | 69238-2296 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Oxycodone Hcl |
Non-Proprietary Name | Oxycodone Hcl |
Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20220401 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA022272 |
Manufacturer | Amneal Pharmaceuticals NY LLC |
Substance Name | OXYCODONE HYDROCHLORIDE |
Strength | 20 |
Strength Unit | mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
DEA Schedule | CII |