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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 202637
Company: SUN PHARM
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LANSOPRAZOLE LANSOPRAZOLE 15MG CAPSULE, DELAYED REL PELLETS;ORAL Discontinued None 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
09/13/2013 ORIG-1 Approval

Label is not available on this site.

Supplements
Action Date Submission Supplement Categories or Approval Type Letters, Reviews, Labels, Patient Package Insert Note Url
09/02/2022 SUPPL-18 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

10/20/2020 SUPPL-15 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

10/20/2020 SUPPL-9 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

10/20/2020 SUPPL-8 Labeling-Medication Guide, Labeling-Package Insert

Label is not available on this site.

10/20/2020 SUPPL-6 Labeling-Package Insert

Label is not available on this site.

03/17/2015 SUPPL-5 Labeling-Package Insert

Label is not available on this site.

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