Triamcinolone Acetonide
- Product NDC
- 70518-4582
- 11-digit product format
- 705184582
- Labeler code
- 70518
- Product ID
- 70518-4582_4c9c23a9-bb45-8810-e063-6294a90aaa77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamcinolone Acetonide
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207550
- Marketing category
- ANDA
- Marketing start
- 2026-03-09
- Substance
- TRIAMCINOLONE ACETONIDE
- Active strength
- 400 mg/10mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Triamcinolone Acetonide
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRIAMCINOLONE ACETONIDE | 400 mg/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F446C597KA |
| Rxcui | 1085754 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4582-0 | Triamcinolone Acetonide | 10 mL in 1 VIAL, MULTI-DOSE | INJECTION, SUSPENSION | 10 | | 1 |
| 70518-4582-0 | Triamcinolone Acetonide | 1 in 1 CARTON | INJECTION, SUSPENSION | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4582-0 | 70518458200 | 1 VIAL, MULTI-DOSE in 1 CARTON (70518-4582-0) / 10 mL in 1 VIAL, MULTI-DOSE | 2026-03-09 | No | No | Current |