NDC 47335-235 – Methotrexate

Methotrexate Sodium 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC47335-235

Product details

Brand name
Methotrexate
Generic name
Methotrexate Sodium
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201749
Marketed since
November 10, 2017
Listing expires
December 31, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (2)

Package NDCDescriptionSince
47335-235-83100 TABLET in 1 BOTTLE (47335-235-83)Nov 10, 2017
47335-235-9636 TABLET in 1 BOTTLE (47335-235-96)Nov 10, 2017

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