| NDC Code | 48866-1061-2 | 
|---|
			| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (48866-1061-2) | 
|---|
			| Product NDC | 48866-1061 | 
|---|
			| 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 | 20151101 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA065093 | 
|---|
			| Manufacturer | Lek Pharmaceuticals, d.d. | 
|---|
			| 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] | 
|---|