| NDC Code | 55700-967-60 |
|---|
| Package Description | 60 TABLET in 1 BOTTLE (55700-967-60) |
|---|
| Product NDC | 55700-967 |
|---|
| 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 | 20220503 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207419 |
|---|
| Manufacturer | Quality Care Products, LLC |
|---|
| Substance Name | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
|---|
| Strength | 325; 7.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Full Opioid Agonists [MoA], Opioid Agonist [EPC] |
|---|
| DEA Schedule | CII |
|---|