NDC 71335-2221 – Methotrexate

Methotrexate Sodium 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2221

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210454
Marketed since
January 30, 2020
Listing expires
December 31, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2221-130 TABLET in 1 BOTTLE (71335-2221-1)Aug 15, 2023
71335-2221-212 TABLET in 1 BOTTLE (71335-2221-2)Aug 15, 2023
71335-2221-320 TABLET in 1 BOTTLE (71335-2221-3)Aug 15, 2023
71335-2221-4100 TABLET in 1 BOTTLE (71335-2221-4)Aug 15, 2023
71335-2221-536 TABLET in 1 BOTTLE (71335-2221-5)Aug 15, 2023
71335-2221-624 TABLET in 1 BOTTLE (71335-2221-6)Aug 15, 2023
71335-2221-790 TABLET in 1 BOTTLE (71335-2221-7)Aug 15, 2023
71335-2221-84 TABLET in 1 BOTTLE (71335-2221-8)Aug 15, 2023

Other Methotrexate products