Search by Drug Name or NDC
NDC 71656-0042-16 Triamcinolone Acetonide 1 mg/g Details
Triamcinolone Acetonide 1 mg/g
Triamcinolone Acetonide is a TOPICAL CREAM in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Saptalis Pharmaceuticals, LLC.. The primary component is TRIAMCINOLONE ACETONIDE.
MedlinePlus Drug Summary
Triamcinolone topical is used to treat the itching, redness, dryness, crusting, scaling, inflammation, and discomfort of various skin conditions, including psoriasis (a skin disease in which red, scaly patches form on some areas of the body and eczema (a skin disease that causes the skin to be dry and itchy and to sometimes develop red, scaly rashes). It is also used as a dental paste to relieve the discomfort of mouth sores. Triamcinolone is in a class of medications called corticosteroids. It works by activating natural substances in the skin to reduce swelling, redness, and itching.
Related Packages: 71656-0042-16Last Updated: 05/19/2024
MedLinePlus Full Drug Details: Triamcinolone Topical
Product Information
| NDC | 71656-0042 |
|---|---|
| Product ID | 71656-042_5de11b51-9f0f-4b8f-a010-e3dbf23c42b8 |
| Associated GPIs | |
| GCN Sequence Number | 007594 |
| GCN Sequence Number Description | triamcinolone acetonide CREAM (G) 0.1 % TOPICAL |
| HIC3 | Q5P |
| HIC3 Description | TOPICAL ANTI-INFLAMMATORY STEROIDAL |
| GCN | 31232 |
| HICL Sequence Number | 002891 |
| HICL Sequence Number Description | TRIAMCINOLONE ACETONIDE |
| Brand/Generic | Generic |
| Proprietary Name | Triamcinolone Acetonide |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | triamcinolone acetonide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | CREAM |
| Route | TOPICAL |
| Active Ingredient Strength | 1 |
| Active Ingredient Units | mg/g |
| Substance Name | TRIAMCINOLONE ACETONIDE |
| Labeler Name | Saptalis Pharmaceuticals, LLC. |
| Pharmaceutical Class | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA040671 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 71656-0042-16 (71656004216)
| NDC Package Code | 71656-042-16 |
|---|---|
| Billing NDC | 71656004216 |
| Package | 454 g in 1 JAR (71656-042-16) |
| Marketing Start Date | 2023-08-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |