Triamcinolone Acetonide
- Product NDC
- 71205-451
- 11-digit product format
- 712050451
- Labeler code
- 71205
- Product ID
- 71205-451_160cc186-71e9-4166-972c-00077ac99997
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamcinolone Acetonide
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRAMUSCULAR
- Labeler
- Proficient Rx LP
- Application
- ANDA209852
- Marketing category
- ANDA
- Marketing start
- 2019-08-29
- 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 |
|---|
| 71205-451-01 | 71205045101 | 1 VIAL, SINGLE-DOSE in 1 CARTON (71205-451-01) / 1 mL in 1 VIAL, SINGLE-DOSE | 2020-04-23 | No | No | Historical |