NDC product
Triamcinolone Acetonide
NDC 0703-0243 · Teva Parenteral Medicines, Inc.
Key facts
| Product NDC | 0703-0243 |
|---|---|
| Proprietary name | Triamcinolone Acetonide |
| Nonproprietary name | Triamcinolone Acetonide |
| Substances | TRIAMCINOLONE ACETONIDE |
| Dosage form | INJECTION, SUSPENSION |
| Route | INTRA-ARTICULAR, INTRAMUSCULAR |
| Labeler | Teva Parenteral Medicines, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA209852 |
| Pharmacologic classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
| Marketing start | Aug 29, 2019 |
| Marketing end | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory