NDC 71335-1118 – Methotrexate

Methotrexate Sodium 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1118

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA081235
Marketed since
May 18, 1992
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
71335-1118-130 TABLET in 1 BOTTLE (71335-1118-1)Feb 25, 2019
71335-1118-212 TABLET in 1 BOTTLE (71335-1118-2)May 17, 2024
71335-1118-320 TABLET in 1 BOTTLE (71335-1118-3)May 17, 2024
71335-1118-4100 TABLET in 1 BOTTLE (71335-1118-4)May 17, 2024
71335-1118-536 TABLET in 1 BOTTLE (71335-1118-5)May 17, 2024
71335-1118-624 TABLET in 1 BOTTLE (71335-1118-6)May 17, 2024
71335-1118-790 TABLET in 1 BOTTLE (71335-1118-7)May 17, 2024
71335-1118-84 TABLET in 1 BOTTLE (71335-1118-8)May 17, 2024

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