Triamcinolone Acetonide
- Product NDC
- 72603-108
- 11-digit product format
- 726030108
- Labeler code
- 72603
- Product ID
- 72603-108_a1114479-2818-4f95-828f-6a8da49087d0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Triamcinolone Acetonide
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRAMUSCULAR
- Labeler
- Northstar RxLLC
- Application
- ANDA209852
- Marketing category
- ANDA
- Marketing start
- 2021-03-22
- Marketing end
- 0000-00-00
- Substance
- TRIAMCINOLONE ACETONIDE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72603-108-01 | 72603010801 | 1 VIAL, SINGLE-DOSE in 1 CARTON (72603-108-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2021-03-22 | 0000-00-00 | No | No | Current |