Home NDC 69263-821 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 Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Package NDC Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded product product D Discontinued by firm d630ba8d3edf…732f749b63fb…2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 69263-821-01 D Discontinued by firm d630ba8d3edf…732f749b63fb…2019-12-08 06:16 UTC · source 2019-12-05 excluded product product E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…2019-12-08 06:16 UTC · source 2019-12-05 excluded package package 69263-821-01 E Excluded after deficient or non-compliant submission was not corrected 110d247fa046…a55b01930146…
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded TRIAMCINOLONE ACETONIDE ACTIVE INGREDIENT F446C597KA PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 TRIAMCINOLONE ACETONIDE ACTIVE MOIETY F446C597KA PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 BENZYL ALCOHOL INACTIVE INGREDIENT LKG8494WBH PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 CARBOXYMETHYLCELLULOSE SODIUM INACTIVE INGREDIENT K679OBS311 PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 HYDROCHLORIC ACID INACTIVE INGREDIENT QTT17582CB PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 NITROGEN INACTIVE INGREDIENT N762921K75 PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 SODIUM CHLORIDE INACTIVE INGREDIENT 451W47IQ8X PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1 SODIUM HYDROXIDE INACTIVE INGREDIENT 55X04QC32I PRO-C-DURE 6 KIT (KENALOG) KIT [OAKLOCK, LLC] 1
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