| NDC Code: |
67296-0378 |
| Proprietary Name: |
Propoxyphene Napsylate and Acetaminophen |
| Suffix: |
|
| Non-Proprietary Name: |
Propoxyphene Napsylate and Acetaminophen |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
25-11-2009 |
| Category Name: |
ANDA |
| Application Number: |
ANDA074119 |
| Labeler: |
REDPHARM DRUG INC. |
| Substance Name: |
ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE |
| Active Numerator Strength: |
650; 100 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Full Opioid Agonists [MoA],Opioid Agonist [EPC] |
| DEA Schedule: |
CIV |
