NDC Code | 49999-855-60 |
Package Description | 60 TABLET in 1 BOTTLE (49999-855-60) |
Product NDC | 49999-855 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Oxycodone And Acetaminophen |
Non-Proprietary Name | Oxycodone Hydrochloride And Acetaminophen |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20111115 |
Marketing Category Name | ANDA |
Application Number | ANDA040371 |
Manufacturer | Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC |
Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
Strength | 650; 10 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |