NDC Code | 35356-801-60 |
Package Description | 60 TABLET in 1 BOTTLE (35356-801-60) |
Product NDC | 35356-801 |
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 | 20120802 |
Marketing Category Name | ANDA |
Application Number | ANDA202677 |
Manufacturer | Quality Care Products, LLC |
Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
Strength | 325; 10 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
DEA Schedule | CII |