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) |
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 NDC: | 0781-3245-70 |
Package Description: | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3245-70) > 10 mL in 1 VIAL, MULTI-DOSE |
NDC Code | 0781-3245-70 |
Proprietary Name | Triamcinolone Acetonide |
Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0781-3245-70) > 10 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 |