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Methylprednisolone
Methylprednisolone - 0703-0043-01 - (Methylprednisolone acetate)
Drug Information of Methylprednisolone
| Product NDC: | 0703-0043 |
| Proprietary Name: | Methylprednisolone |
| 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Methylprednisolone
| Product NDC: | 0703-0043 |
| Labeler Name: | Teva Parenteral Medicines, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040620 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20061031 |
Package Information of Methylprednisolone
| Package NDC: | 0703-0043-01 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0043-01) > 5 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Methylprednisolone
| NDC Code | 0703-0043-01 |
| Proprietary Name | Methylprednisolone |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0043-01) > 5 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0703-0043 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Methylprednisolone acetate |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
| Start Marketing Date | 20061031 |
| 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] |
