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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 211003
Company: MEITHEAL
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
LEVOLEUCOVORIN CALCIUM LEVOLEUCOVORIN CALCIUM EQ 50MG BASE/VIAL POWDER;INTRAVENOUS 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
08/22/2019 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
09/22/2023 SUPPL-3 Labeling-Package Insert

Label is not available on this site.

09/22/2023 SUPPL-2 Labeling-Package Insert

Label is not available on this site.

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