| NDC Code: |
50436-6051 |
| Proprietary Name: |
Amoxicillin and Clavulanate Potassium |
| Suffix: |
|
| Non-Proprietary Name: |
Amoxicillin and Clavulanate Potassium |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
16-11-2011 |
| Category Name: |
ANDA |
| Application Number: |
ANDA065101 |
| Labeler: |
UNIT DOSE SERVICES |
| Substance Name: |
AMOXICILLIN; CLAVULANATE POTASSIUM |
| Active Numerator Strength: |
500; 125 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
| DEA Schedule: |
|
