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Methylprednisolone Acetate
Methylprednisolone Acetate - 0703-0031-04 - (Methylprednisolone Acetate)
Drug Information of Methylprednisolone Acetate
| Product NDC: | 0703-0031 |
| 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) |
Labeler Information of Methylprednisolone Acetate
| Product NDC: | 0703-0031 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040557 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050308 |
Package Information of Methylprednisolone Acetate
| Package NDC: | 0703-0031-04 |
| Package Description: | 25 VIAL, GLASS in 1 CARTON (0703-0031-04) > 1 mL in 1 VIAL, GLASS |
NDC Information of Methylprednisolone Acetate
| NDC Code | 0703-0031-04 |
| Proprietary Name | Methylprednisolone Acetate |
| Package Description | 25 VIAL, GLASS in 1 CARTON (0703-0031-04) > 1 mL in 1 VIAL, GLASS |
| Product NDC | 0703-0031 |
| 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 | 20050308 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | METHYLPREDNISOLONE ACETATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
