| NDC Code: |
50436-0264 |
| Proprietary Name: |
Etodolac |
| Suffix: |
|
| Non-Proprietary Name: |
Etodolac |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
30-12-2010 |
| Category Name: |
ANDA |
| Application Number: |
ANDA075665 |
| Labeler: |
UNIT DOSE SERVICES |
| Substance Name: |
ETODOLAC |
| Active Numerator Strength: |
500 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
| DEA Schedule: |
|
