| NDC Code: |
0781-1619 |
| Proprietary Name: |
Amoxicillin and Clavulanate Potassium |
| Suffix: |
|
| Non-Proprietary Name: |
Amoxicillin and Clavulanate Potassium |
| Dosage Form: |
TABLET, CHEWABLE |
| Method: |
ORAL |
| Original Marketing Date: |
18-04-2002 |
| Category Name: |
ANDA |
| Application Number: |
ANDA065065 |
| Labeler: |
SANDOZ INC |
| Substance Name: |
AMOXICILLIN; CLAVULANATE POTASSIUM |
| Active Numerator Strength: |
200; 28.5 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA],Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient] |
| DEA Schedule: |
|
