| NDC Code | 55700-976-90 | 
|---|
			| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55700-976-90) | 
|---|
			| Product NDC | 55700-976 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Metoprolol Succinate | 
|---|
			
			| Non-Proprietary Name | Metoprolol Succinate Er Tablets | 
|---|
			| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20220719 | 
|---|
			| End Marketing Date | 20250930 | 
|---|
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA211143 | 
|---|
			| Manufacturer | Quality Care Products, LLC | 
|---|
			| Substance Name | METOPROLOL SUCCINATE | 
|---|
			| Strength | 25 | 
|---|
			| Strength Unit | mg/1 | 
|---|
			| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC] | 
|---|