NDC 69621-846

Yaliira Pak

Triamcinolone Acetonide, Dimethicone

Yaliira Pak is a Kit in the Human Prescription Drug category. It is labeled and distributed by Shoreline Pharmaceuticals. The primary component is .

Product ID69621-846_9db9f00e-236f-4198-882f-412c8016ad24
NDC69621-846
Product TypeHuman Prescription Drug
Proprietary NameYaliira Pak
Generic NameTriamcinolone Acetonide, Dimethicone
Dosage FormKit
Marketing Start Date2016-12-29
Marketing CategoryANDA / ANDA
Application NumberANDA205373
Labeler NameShoreline Pharmaceuticals
Active Ingredient Strength0
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 69621-846-00

1 KIT in 1 CARTON (69621-846-00) * 80 g in 1 TUBE (52565-014-80) * 118 mL in 1 TUBE (59088-333-08)
Marketing Start Date2016-12-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69621-846-00 [69621084600]

Yaliira Pak KIT
Marketing CategoryANDA
Application NumberANDA205373
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-29
Marketing End Date2019-04-16

Drug Details

OpenFDA Data

SPL SET ID:f92f88cd-308a-48d4-8228-ca3704b6b39e
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 1085636
  • 259090
  • NDC Crossover Matching brand name "Yaliira Pak" or generic name "Triamcinolone Acetonide, Dimethicone"

    NDCBrand NameGeneric Name
    69621-846Yaliira Paktriamcinolone acetonide, dimethicone
    59088-846Ellzia Paktriamcinolone acetonide, dimethicone
    70859-054NuTriaRX CreamPakTRIAMCINOLONE ACETONIDE, dimethicone
    71574-501ScarzenTriamcinolone Acetonide, Dimethicone
    69837-003Sure ResultTAC PakTRIAMCINOLONE ACETONIDE, DIMETHICONE

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.