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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 206055
Company: ZYDUS PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM EQ 20MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription AB No No
ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM EQ 40MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription AB No No
Original Approvals or Tentative Approvals
Action Date Submission Action Type Submission Classification Review Priority; Orphan Status Letters, Reviews, Labels, Patient Package Insert Notes Url
06/07/2023 ORIG-1 Approval STANDARD

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
11/08/2023 SUPPL-2 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

ESOMEPRAZOLE MAGNESIUM

FOR SUSPENSION, DELAYED RELEASE;ORAL; EQ 20MG BASE/PACKET
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM EQ 20MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription No AB 211751 CIPLA
ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM EQ 20MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription No AB 206055 ZYDUS PHARMS
NEXIUM ESOMEPRAZOLE MAGNESIUM EQ 20MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription Yes AB 021957 ASTRAZENECA

FOR SUSPENSION, DELAYED RELEASE;ORAL; EQ 40MG BASE/PACKET
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM EQ 40MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription No AB 211751 CIPLA
ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM EQ 40MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription No AB 206055 ZYDUS PHARMS
NEXIUM ESOMEPRAZOLE MAGNESIUM EQ 40MG BASE/PACKET FOR SUSPENSION, DELAYED RELEASE;ORAL Prescription Yes AB 021957 ASTRAZENECA
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