NDC 71335-1772 – Methotrexate

Methotrexate Sodium 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1772

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213343
Marketed since
August 24, 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
71335-1772-130 TABLET in 1 BOTTLE (71335-1772-1)Dec 29, 2021
71335-1772-212 TABLET in 1 BOTTLE (71335-1772-2)Dec 29, 2021
71335-1772-320 TABLET in 1 BOTTLE (71335-1772-3)Dec 29, 2021
71335-1772-4100 TABLET in 1 BOTTLE (71335-1772-4)Dec 29, 2021
71335-1772-536 TABLET in 1 BOTTLE (71335-1772-5)Dec 29, 2021
71335-1772-624 TABLET in 1 BOTTLE (71335-1772-6)Jan 21, 2021
71335-1772-790 TABLET in 1 BOTTLE (71335-1772-7)Dec 29, 2021
71335-1772-84 TABLET in 1 BOTTLE (71335-1772-8)Dec 29, 2021

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