NDC Code | 45865-856-40 |
Package Description | 40 TABLET in 1 BOTTLE (45865-856-40) |
Product NDC | 45865-856 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Oxycodone And Acetaminophen |
Non-Proprietary Name | Oxycodone And Acetaminophen |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20120117 |
Marketing Category Name | ANDA |
Application Number | ANDA202677 |
Manufacturer | Medsource Pharmaceuticals |
Substance Name | OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN |
Strength | 10; 325 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |