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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 088937
Company: ABRAXIS PHARM

Products on ANDA 088937

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
METHOTREXATE SODIUM	METHOTREXATE SODIUM	EQ 100MG BASE/VIAL	INJECTABLE;INJECTION	Discontinued	None	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 088937

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
08/27/1987	SUPPL-1	Manufacturing (CMC)		Label is not available on this site.

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