KENALOG-40
- Product NDC
- 70518-0075
- 11-digit product format
- 705180075
- Labeler code
- 70518
- Product ID
- 70518-0075_d2a806c7-058f-d2b1-e053-2995a90a6ed6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TRIAMCINOLONE ACETONIDE
- Dosage form
- INJECTION, SUSPENSION
- Route
- INTRA-ARTICULAR; INTRAMUSCULAR
- Labeler
- REMEDYREPACK INC.
- Application
- NDA014901
- Marketing category
- NDA
- Marketing start
- 2016-12-21
- Marketing end
- 0000-00-00
- Substance
- TRIAMCINOLONE ACETONIDE
- Active strength
- 40 mg/mL
- Pharmacologic classes
- Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0075 | KENALOG-40 (TRIAMCINOLONE ACETONIDE) INJECTION, SUSPENSION [REMEDYREPACK INC.] | 8 | Legacy NDC | 20211209_c29c69a5-83a0-45f3-a8e9-61fc9cf9705e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0075-0 | 70518007500 | 1 VIAL, SINGLE-DOSE in 1 CARTON (70518-0075-0) > 1 mL in 1 VIAL, SINGLE-DOSE | 2016-12-21 | 0000-00-00 | No | No | Current |