Pro-C-Dure 6 Kit
- Product NDC
- 76420-622
- 11-digit product format
- 764200622
- Labeler code
- 76420
- Product ID
- 76420-622_07064ca3-dc6a-0927-e063-6294a90aac46
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- kenalog
- Dosage form
- KIT
- Route
- INTRA-ARTICULAR; INTRAMUSCULAR
- Labeler
- Asclemed USA, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-08-17
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Pro-C-Dure 6 Kit
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 1792144 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70121-1049-2 | Pro-C-Dure 6 Kit | 1 mL in 1 VIAL | INJECTION, SUSPENSION | 3 mL | 40 mg in 1mL | 1 |
| 70121-1049-2 | Pro-C-Dure 6 Kit | 1 in 1 CARTON | INJECTION, SUSPENSION | | 40 mg in 1mL | 1 |
| 76420-622-01 | Pro-C-Dure 6 Kit | 1 in 1 CARTON | KIT | 1 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76420-622 | PRO-C-DURE 6 KIT (KENALOG) KIT [ASCLEMED USA, INC.] | 1 | Current NDC, 3 package rows | 20231006_3c627313-948f-4867-b64a-8e9adc40c405.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70121-1049-2 | 70121104902 | 1 mL in 1 VIAL | 1 ml | | | | Historical |
| 76420-622-01 | 76420062201 | 1 KIT in 1 CARTON (76420-622-01) * 1 VIAL in 1 CARTON (70121-1049-2) / 1 mL in 1 VIAL | 1 kit | 2023-10-04 | No | No | Historical |