NDC Code | 55700-658-60 |
Package Description | 60 TABLET in 1 BOTTLE (55700-658-60) |
Product NDC | 55700-658 |
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 | 20180720 |
Marketing Category Name | ANDA |
Application Number | ANDA090535 |
Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | OXYCODONE HYDROCHLORIDE; ACETAMINOPHEN |
Strength | 5; 325 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
DEA Schedule | CII |