NDC Code | 60760-200-10 |
Package Description | 10 TABLET in 1 BOTTLE, PLASTIC (60760-200-10) |
Product NDC | 60760-200 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Oxycodone Hydrochloride And Acetaminophen |
Non-Proprietary Name | Oxycodone Hydrochloride And Acetaminophen |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20090608 |
Marketing Category Name | ANDA |
Application Number | ANDA040777 |
Manufacturer | St. Mary's Medical Park Pharmacy |
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 |