| NDC Code | 55700-751-20 | 
|---|
			| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (55700-751-20) | 
|---|
			| Product NDC | 55700-751 | 
|---|
			| 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 | 20190510 | 
|---|
			| End Marketing Date | 20211031 | 
|---|
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA204755 | 
|---|
			| Manufacturer | Quality Care Products, LLC | 
|---|
			| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM | 
|---|
			| Strength | 875; 125 | 
|---|
			| Strength Unit | mg/1; mg/1 | 
|---|
			| Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] | 
|---|