NDC 59088-723

CeleXib 100-EZS

Celecoxib

CeleXib 100-EZS is a Kit in the Human Prescription Drug category. It is labeled and distributed by Puretek Corporation. The primary component is .

Product ID59088-723_c9b6f563-df3a-46d5-8619-ff781ba4a39f
NDC59088-723
Product TypeHuman Prescription Drug
Proprietary NameCeleXib 100-EZS
Generic NameCelecoxib
Dosage FormKit
Marketing Start Date2018-10-22
Marketing CategoryANDA / ANDA
Application NumberANDA204519
Labeler NamePureTek Corporation
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 59088-723-00

1 KIT in 1 KIT (59088-723-00) * 100 CAPSULE in 1 BOTTLE (62332-141-31) * 59 mL in 1 BOTTLE, SPRAY (GS1:7-31477-27221-7)
Marketing Start Date2018-10-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59088-723-00 [59088072300]

CeleXib 100-EZS KIT
Marketing CategoryANDA
Application NumberANDA204519
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-10-22
Marketing End Date2019-04-15

Drug Details

OpenFDA Data

SPL SET ID:354dca74-b468-4fff-8442-90fb5b95948e
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 205322
    • UPC Code
  • 0731477272217

    • NDC Crossover Matching brand name "CeleXib 100-EZS" or generic name "Celecoxib"

    NDCBrand NameGeneric Name
    59088-723CeleXib 100-EZSCeleXib 100-EZS
    0025-1515CELEBREXCelecoxib
    0025-1520CELEBREXCelecoxib
    0025-1525CELEBREXCelecoxib
    0025-1530CELEBREXCelecoxib
    0093-7165CelecoxibCelecoxib
    0093-7166CelecoxibCelecoxib
    0093-7170CelecoxibCelecoxib
    0093-7306CelecoxibCelecoxib
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.