NDC 0904-7141 – Methotrexate

Methotrexate 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0904-7141

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Major Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207812
Marketed since
February 9, 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 (1)

Package NDCDescriptionSince
0904-7141-1020 BLISTER PACK in 1 CARTON (0904-7141-10) / 1 TABLET in 1 BLISTER PACKFeb 9, 2017

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