| NDC Code: |
63481-621 |
| Proprietary Name: |
PERCOCET |
| Suffix: |
|
| Non-Proprietary Name: |
oxycodone hydrochloride and acetaminophen |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
30-07-1999 |
| End of Marketing: |
31-12-2013 |
| Category Name: |
ANDA |
| Application Number: |
ANDA040341 |
| Labeler: |
ENDO PHARMACEUTICALS |
| Substance Name: |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Active Numerator Strength: |
500; 7.5 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: |
CII |
