JTT Physicians

Product NDC
49836-524
11-digit product format
498360524
Labeler code
49836
Product ID
49836-524_32b6efe4-b29c-48e5-b812-802ae6bf41ad
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
triamcinolone acetonide,lidocaine hydrochloride, povidone iodine, ammonia
Dosage form
KIT
Labeler
RX PHARMA-PACK, INC.
Application
NDA014901
Marketing category
NDA
Marketing start
2015-10-26
Marketing end
0000-00-00
Active strength
0
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49836-524-01EA - Each49836-524fc553c34-9e27-4143-9f62-72fdb57baeae12016-01-13