Triamcinolone acetonide
- Product NDC
- 80425-0262
- 11-digit product format
- 804250262
- Labeler code
- 80425
- Product ID
- 80425-0262_2a9b7c00-1681-4da0-e063-6394a90a926d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamcinolone acetonide
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRAMUSCULAR
- Labeler
- Advanced Rx Pharmacy of Tennessee, LLC
- Application
- ANDA209852
- Marketing category
- ANDA
- Marketing start
- 2023-02-15
- Substance
- TRIAMCINOLONE ACETONIDE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F446C597KA | TRIAMCINOLONE ACETONIDE | 76-25-5 | TRIAMCINOLONE ACETONIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 80425-0262-1 | 80425026201 | 1 VIAL, MULTI-DOSE in 1 CARTON (80425-0262-1) / 5 mL in 1 VIAL, MULTI-DOSE | 2023-02-15 | No | No | Historical |