| NDC Code: |
59630-777 |
| Proprietary Name: |
Naprelan |
| Suffix: |
|
| Non-Proprietary Name: |
Naproxen Sodium |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
01-04-1996 |
| Category Name: |
NDA |
| Application Number: |
NDA020353 |
| Labeler: |
SHIONOGI INC. |
| Substance Name: |
NAPROXEN SODIUM |
| Active Numerator Strength: |
750 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule: |
|
