Triasil
- Product NDC
- 59088-730
- 11-digit product format
- 590880730
- Labeler code
- 59088
- Product ID
- 59088-730_f3095546-7f72-2665-e053-2995a90aff07
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamcinolone Acetonide
- Dosage form
- KIT
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-01-20
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Triasil
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 1085636 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 45802-055-36 | Triasil | 1 in 1 CARTON | OINTMENT | | 1 mg in 1g | 2 |
| 45802-055-36 | Triasil | 80 g in 1 TUBE | OINTMENT | 80 g | 1 mg in 1g | 2 |
| 59088-730-00 | Triasil | 1 in 1 KIT | KIT | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-730 | TRIASIL (TRIAMCINOLONE ACETONIDE) KIT [PURETEK CORPORATION] | 2 | Current NDC, 3 package rows | 20230202_dcf6c630-6f5d-3d2f-e053-2995a90ad812.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 45802-055-36 | 45802005536 | 1 in 1 CARTON | | | | | Historical |
| 59088-730-00 | 59088073000 | 1 KIT in 1 KIT (59088-730-00) * 1 TUBE in 1 CARTON (45802-055-36) / 80 g in 1 TUBE | 1 kit | 2023-01-20 | No | No | Current |