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Aristocort
Aristocort - 0781-3037-75 - (Triamcinolone Diacetate)
Drug Information of Aristocort
| Product NDC: | 0781-3037 |
| Proprietary Name: | Aristocort |
| Non Proprietary Name: | Triamcinolone Diacetate |
| Active Ingredient(s): | 40 mg/mL & nbsp; Triamcinolone Diacetate |
| Administration Route(s): | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; PARENTERAL |
| Dosage Form(s): | INJECTION, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Aristocort
| Product NDC: | 0781-3037 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA012802 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19610905 |
Package Information of Aristocort
| Package NDC: | 0781-3037-75 |
| Package Description: | 1 VIAL in 1 CARTON (0781-3037-75) > 5 mL in 1 VIAL |
NDC Information of Aristocort
| NDC Code | 0781-3037-75 |
| Proprietary Name | Aristocort |
| Package Description | 1 VIAL in 1 CARTON (0781-3037-75) > 5 mL in 1 VIAL |
| Product NDC | 0781-3037 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Triamcinolone Diacetate |
| Dosage Form Name | INJECTION, SUSPENSION |
| Route Name | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; PARENTERAL |
| Start Marketing Date | 19610905 |
| Marketing Category Name | NDA |
| Labeler Name | Sandoz Inc |
| Substance Name | TRIAMCINOLONE DIACETATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
