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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 217738
Company: SCIEGEN PHARMS INC
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;375MG TABLET, DELAYED RELEASE;ORAL Prescription AB No No
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;500MG TABLET, 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
10/11/2023 ORIG-1 Approval STANDARD

Label is not available on this site.

NAPROXEN AND ESOMEPRAZOLE MAGNESIUM

TABLET, DELAYED RELEASE;ORAL; EQ 20MG BASE;375MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;375MG TABLET, DELAYED RELEASE;ORAL Prescription No AB 213699 AJANTA PHARMA LTD
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;375MG TABLET, DELAYED RELEASE;ORAL Prescription No AB 204206 DR REDDYS
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;375MG TABLET, DELAYED RELEASE;ORAL Prescription No AB 217738 SCIEGEN PHARMS INC

TABLET, DELAYED RELEASE;ORAL; EQ 20MG BASE;500MG
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;500MG TABLET, DELAYED RELEASE;ORAL Prescription No AB 213699 AJANTA PHARMA LTD
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;500MG TABLET, DELAYED RELEASE;ORAL Prescription No AB 204206 DR REDDYS
NAPROXEN AND ESOMEPRAZOLE MAGNESIUM ESOMEPRAZOLE MAGNESIUM; NAPROXEN EQ 20MG BASE;500MG TABLET, DELAYED RELEASE;ORAL Prescription No AB 217738 SCIEGEN PHARMS INC
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