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Triamcinolone Acetonide
Triamcinolone Acetonide - 0781-3245-75 - (Triamcinolone Acetonide)
Drug Information of Triamcinolone Acetonide
| Product NDC: | 0781-3245 |
| Proprietary Name: | Triamcinolone Acetonide |
| Non Proprietary Name: | Triamcinolone Acetonide |
| Active Ingredient(s): | 40 mg/mL & nbsp; Triamcinolone Acetonide |
| Administration Route(s): | INTRA-ARTICULAR; INTRAMUSCULAR |
| Dosage Form(s): | INJECTION, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Triamcinolone Acetonide
| Product NDC: | 0781-3245 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090164 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090527 |
Package Information of Triamcinolone Acetonide
| Package NDC: | 0781-3245-75 |
| Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3245-75) > 5 mL in 1 VIAL, MULTI-DOSE |
NDC Information of Triamcinolone Acetonide
| NDC Code | 0781-3245-75 |
| Proprietary Name | Triamcinolone Acetonide |
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3245-75) > 5 mL in 1 VIAL, MULTI-DOSE |
| Product NDC | 0781-3245 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Triamcinolone Acetonide |
| Dosage Form Name | INJECTION, SUSPENSION |
| Route Name | INTRA-ARTICULAR; INTRAMUSCULAR |
| Start Marketing Date | 20090527 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | TRIAMCINOLONE ACETONIDE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
