Pro-C-Dure 6 Kit
- Product NDC
- 69263-821
- 11-digit product format
- 692630821
- Labeler code
- 69263
- Product ID
- 69263-821_cbc4601f-dfcd-253a-e053-2995a90a7a7d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- kenalog
- Dosage form
- KIT
- Route
- INTRA-ARTICULAR; INTRAMUSCULAR
- Labeler
- Oaklock, LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2015-08-17
- Marketing end
- 0000-00-00
- Active strength
- 0
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69263-821 | PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] | 6 | Legacy NDC | 20241019_1129a728-b619-4cf8-8fc8-13bf1ef8a8fb.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69263-821-01 | 69263082101 | 1 KIT in 1 CARTON (69263-821-01) * 1 VIAL, SINGLE-DOSE in 1 CARTON (0003-0293-05) > 1 mL in 1 VIAL, SINGLE-DOSE | 1 kit | 2015-08-17 | 0000-00-00 | No | No | Current |