Product Specifications
| Specification | Details |
| Manufacturer / Brand | Amneal Biosciences LLC |
| Manufacturer # / SKU | 70121116801 |
| NDC Number | 70121-1168-01 |
| Active Ingredient | Triamcinolone Acetonide |
| Concentration | 40 mg / mL |
| Total Volume | 5 mL (200 mg total per vial) |
| Container Type | Multi-Dose Vial (MDV) |
| Application | Glucocorticoid / Anti-inflammatory |
| Route of Admin | Intramuscular (IM) / Intra-articular |
| Storage | Store at 20°C to 25°C; Do Not Freeze |
| Packaging / Sold As | Individual 5 mL Vial |
| UNSPSC Code | 51101807 |
Key Features
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Multi-Dose Efficiency: The 5 mL vial allows for multiple doses to be drawn from a single container, making it a cost-effective choice for busy clinics performing regular joint injections.
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Extended Duration: Like other triamcinolone suspensions, it provides long-lasting therapeutic effects, often sustained over several weeks from a single injection.
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Preserved Formula: Contains benzyl alcohol (0.99%) as a preservative, which is standard for multi-dose vials to prevent microbial growth during repeated access.
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Liquid Suspension: Consists of micronized powder in liquid form; the product appears as an opaque, milky-white liquid.
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AB-Rated Generic: A therapeutic equivalent to Kenalog®-40, ensuring the same clinical efficacy and safety profile.
Clinical Applications
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Joint Care: Primarily used for intra-articular injection to treat rheumatoid arthritis, osteoarthritis, and acute bursitis.
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Systemic Therapy: Administered deep intramuscularly for severe allergic reactions or dermatologic conditions when oral therapy is insufficient.
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Soft Tissue: Effective for intralesional treatment of keloids and localized inflammatory lesions.
⚠️ Handling Note: As a suspension, the vial must be shaken well before each use to ensure the micronized powder is evenly distributed.
⚠️ Strict Warning: Not for Intravenous (IV) use. The particulate matter in the suspension can cause severe vascular complications if injected into a vein.
⚠️ Safety: Because this is a multi-dose vial, strict aseptic technique must be followed during every withdrawal. Discard the vial according to facility policy (typically 28 days after first puncture) or the manufacturer’s expiration.







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