High Outlier
Strength
2.5 mg/mL
Manufacturer
Azurity Pharmaceuticals Inc.NDC
52652200106
Classification
Brand
Dosage Form
SOLUTION
Route
ORAL
Last Updated
1/1/2025
Active Ingredients
METHOTREXATEApproval Type
New Drug (NDA)
FDA Application
NDA208400On Market Since
5/1/2017
Pharmacological Classes
Folate Analog Metabolic Inhibitor
Folic Acid Metabolism Inhibitors
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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