NDC 71335-0782 – Methotrexate

Methotrexate Sodium 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0782

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA081099
Marketed since
November 1, 1990
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (8)

Package NDCDescriptionSince
71335-0782-130 TABLET in 1 BOTTLE (71335-0782-1)Feb 25, 2019
71335-0782-212 TABLET in 1 BOTTLE (71335-0782-2)Apr 9, 2021
71335-0782-320 TABLET in 1 BOTTLE (71335-0782-3)Apr 9, 2021
71335-0782-4100 TABLET in 1 BOTTLE (71335-0782-4)Apr 19, 2018
71335-0782-536 TABLET in 1 BOTTLE (71335-0782-5)Apr 9, 2021
71335-0782-624 TABLET in 1 BOTTLE (71335-0782-6)Apr 9, 2021
71335-0782-790 TABLET in 1 BOTTLE (71335-0782-7)Apr 9, 2021
71335-0782-84 TABLET in 1 BOTTLE (71335-0782-8)Apr 9, 2021

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