| Product NDC: | 54868-0590 |
| Proprietary Name: | Methylprednisolone Acetate |
| Non Proprietary Name: | Methylprednisolone Acetate |
| Active Ingredient(s): | 40 mg/mL & nbsp; Methylprednisolone Acetate |
| Administration Route(s): | INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
| Dosage Form(s): | INJECTION, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-0590 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040557 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120726 |
| Package NDC: | 54868-0590-0 |
| Package Description: | 1 VIAL, GLASS in 1 CARTON (54868-0590-0) > 1 mL in 1 VIAL, GLASS |
| NDC Code | 54868-0590-0 |
| Proprietary Name | Methylprednisolone Acetate |
| Package Description | 1 VIAL, GLASS in 1 CARTON (54868-0590-0) > 1 mL in 1 VIAL, GLASS |
| Product NDC | 54868-0590 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylprednisolone Acetate |
| Dosage Form Name | INJECTION, SUSPENSION |
| Route Name | INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
| Start Marketing Date | 20120726 |
| Marketing Category Name | ANDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | METHYLPREDNISOLONE ACETATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |