Triamcinolone Acetonide
- Product NDC
- 49999-150
- Requested package NDC
- 49999-150-15
- 11-digit product format
- 499990150
- Labeler code
- 49999
- Product ID
- 49999-150_2552e5b6-aaaf-438a-90e6-55db6882f5cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamcinolone Acetonide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA086414
- Marketing category
- ANDA
- Marketing start
- 2012-03-20
- Marketing end
- 0000-00-00
- Substance
- TRIAMCINOLONE ACETONIDE
- Active strength
- 1 mg/g
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 49999-150 | 49999-150-15 | D | Discontinued by firm | 2026-08-03 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Snapshot | Source SHA-256 |
|---|---|---|
| 2025-12-14 17:58 UTC · source 2025-12-05 | d630ba8d3edf… | 732f749b63fb… |
| 2025-08-27 00:01 UTC · source 2025-08-26 | f5e01cc5f278… | a2eaf40c39c3… |
| 2025-04-01 02:39 UTC · source 2025-03-31 | 2ef7874e63bc… | 57b86245f4fa… |
| 2025-03-28 20:22 UTC · source 2025-03-28 | a1b67e2a42f9… | c4cf2c586c0d… |
| 2025-03-22 03:12 UTC · source 2025-03-21 | cfe11265f3b6… | 090c488252e2… |
| 2025-03-10 12:48 UTC · source 2025-03-10 | cdf11ea48f46… | ba0047e9e063… |
| 2025-02-02 03:52 UTC · source 2025-01-31 | 302b2466d912… | e7b80fea0513… |
| 2025-01-20 13:05 UTC · source 2025-01-20 | ed331223b511… | 672a5bd82f5f… |
| 2025-01-11 03:41 UTC · source 2025-01-10 | 0efc9e666f02… | f202fb6c5f17… |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 49999-150-15 | GM - Gram | 49999-150 | d33679ff-5aef-49be-b33f-56c54abb0b24 | 1 | 2012-07-24 |
| 49999-150-30 | GM - Gram | 49999-150 | 9c91327f-8785-445a-87d2-dfadb6358e36 | 1 | 2012-07-24 |
| 49999-150-80 | GM - Gram | 49999-150 | 5ab08322-0365-4ff1-a9b2-95555495336d | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Triamcinolone Acetonide | TRIAMCINOLONE ACETONIDE | NuCare Pharmaceuticals,Inc. | 5439cd3c-da8d-3b96-e054-00144ff8d46c | 2026-01-21 | Adverse reactions | 086414 ANDA086414 |
| Triamcinolone Acetonide | TRIAMCINOLONE ACETONIDE | NuCare Pharmaceuticals,Inc. | 696cd64f-28dd-3dae-e053-2a91aa0a0c76 | 2025-02-13 | Adverse reactions | 086414 ANDA086414 |
| Triamcinolone Acetonide | TRIAMCINOLONE ACETONIDE | Proficient Rx LP | 4aa792cc-7cd4-4a98-8730-fa36feaa9b7a | 2023-02-01 | Adverse reactions | 086414 ANDA086414 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 49999-150-15 | 49999015015 | 1 TUBE in 1 CARTON (49999-150-15) > 15 g in 1 TUBE | 1 tube | 2012-03-20 | 0000-00-00 | No | No | Current |