| NDC Code | 58118-0009-2 |
|---|
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (58118-0009-2) |
|---|
| Product NDC | 58118-0009 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Non-Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19961002 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA050720 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
|---|
| Strength | 875; 125 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
|---|