NDC 0555-0572 – Methotrexate

Methotrexate Sodium 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0555-0572

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA081099
Marketed since
November 1, 1990
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
0555-0572-02100 TABLET in 1 BOTTLE (0555-0572-02)Nov 1, 1990
0555-0572-3536 TABLET in 1 BOTTLE (0555-0572-35)Nov 1, 1990

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