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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 207812
Company: ZYDUS PHARMS
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;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
01/13/2017 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
11/08/2021 SUPPL-4 Labeling-Package Insert, Labeling-Patient Package Insert

Label is not available on this site.

11/08/2021 SUPPL-2 Labeling-Package Insert, Labeling-Patient Package Insert

Label is not available on this site.

METHOTREXATE SODIUM

TABLET;ORAL; EQ 2.5MG BASE
TE Code = AB

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status RLD TE Code Application No. Company
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 213343 ACCORD HLTHCARE
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 210040 AMNEAL PHARMS
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 081099 BARR
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 213362 DAITO
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 210454 EUGIA PHARMA
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 040054 HIKMA
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 081235 MYLAN
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 201749 SUN PHARM
METHOTREXATE SODIUM METHOTREXATE SODIUM EQ 2.5MG BASE TABLET;ORAL Prescription No AB 207812 ZYDUS PHARMS
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