| NDC Code | 60219-1573-1 | 
|---|
			| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (60219-1573-1)  / 1 mL in 1 VIAL, SINGLE-DOSE | 
|---|
			| Product NDC | 60219-1573 | 
|---|
			| Product Type Name | HUMAN PRESCRIPTION DRUG | 
|---|
			| Proprietary Name | Methylprednisolone Acetate | 
|---|
			
			| Non-Proprietary Name | Methylprednisolone Acetate | 
|---|
			| Dosage Form | INJECTION, SUSPENSION | 
|---|
			| Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE | 
|---|
			| Start Marketing Date | 20220410 | 
|---|
			
			| Marketing Category Name | ANDA | 
|---|
			| Application Number | ANDA210043 | 
|---|
			| Manufacturer | Amneal Pharmaceuticals NY LLC | 
|---|
			| Substance Name | METHYLPREDNISOLONE ACETATE | 
|---|
			| Strength | 40 | 
|---|
			| Strength Unit | mg/mL | 
|---|
			| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] | 
|---|