| NDC Code: |
42549-618 |
| Proprietary Name: |
Oxycodone Hydrochloride and Acetaminophen |
| Suffix: |
|
| Non-Proprietary Name: |
Oxycodone Hydrochloride and Acetaminophen |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
01-07-2008 |
| Category Name: |
ANDA |
| Application Number: |
ANDA040778 |
| Labeler: |
STAT RX USA LLC |
| Substance Name: |
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Active Numerator Strength: |
325; 5 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: |
CII |
