NDC 59088-701

PharmapureRx ESOMEP-EZS

Esomeprazole Magnesium

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

Product ID59088-701_b3ca6688-8f5b-3e2f-e053-2995a90a190c
NDC59088-701
Product TypeHuman Prescription Drug
Proprietary NamePharmapureRx ESOMEP-EZS
Generic NameEsomeprazole Magnesium
Dosage FormKit
Marketing Start Date2017-07-26
Marketing CategoryUNAPPROVED DRUG OTHER / ANDA
Application NumberANDA078003
Labeler NamePureTek Corporation
Active Ingredient Strength0
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 59088-701-00

1 KIT in 1 KIT (59088-701-00) * 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0093-6450-56)
Marketing Start Date2017-07-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59088-701-00 [59088070100]

PharmapureRx ESOMEP-EZS KIT
Marketing CategoryANDA
Application NumberANDA078003
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-07-26

Drug Details

OpenFDA Data

SPL SET ID:7115f8c5-9613-4cdc-8cfe-78ef922c3acb
Manufacturer
RxNorm Concept Unique ID - RxCUI
  • 606726
  • NDC Crossover Matching brand name "PharmapureRx ESOMEP-EZS" or generic name "Esomeprazole Magnesium"

    NDCBrand NameGeneric Name
    59088-701PharmapureRx ESOMEP-EZSPharmapureRx ESOMEP-EZS
    0093-6450Esomeprazole MagnesiumEsomeprazole Magnesium
    0093-6451Esomeprazole MagnesiumEsomeprazole Magnesium
    0186-0382Esomeprazole magnesiumEsomeprazole magnesium
    0186-0384Esomeprazole magnesiumEsomeprazole magnesium
    0186-4010NEXIUMEsomeprazole magnesium
    0186-4020NEXIUMEsomeprazole magnesium
    0186-4025NEXIUMEsomeprazole magnesium

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