Methotrexate — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

METHOTREXATE SODIUM

Base moiety

METHOTREXATE

RxNorm CUI

105586

UNII

3IG1E710ZN

Medication products

10

Brand names

4

Dosage forms

6

FAERS reports

489,790 · not a risk measure

Products containing this ingredient

Source: NDC Directory 10 products

Methotrexate Disodium Injection
1 NDC
Methotrexate Disodium Powder
1 NDC
Methotrexate Disodium Salt Powder
1 NDC
METHOTREXATE SODIUM Methotrexate Sodium · Powder
3 NDC
Methotrexate Tablet
Rx ANDA TE AB Shortage 27 NDC
Methotrexate Injection, Powder, Lyophilized, for Solution
Rx ANDA TE AP 3 NDC
Methotrexate Injection, Solution
Rx ANDA TE AP 2 recalls 16 NDC
Methotrexate Sodium Tablet
Rx ANDA TE AB 1 recall 2 NDC
Rasuvo methotrexate · Injection, Solution
Rx NDA 9 NDC
Trexall Methotrexate · Tablet, Film Coated
Rx ANDA 4 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	3	Methotrexate Disodium, Methotrexate Disodium Salt, METHOTREXATE SODIUM
Tablet	2	Methotrexate, Methotrexate Sodium
INJECTION, Solution	2	Methotrexate, Rasuvo
Injection	1	Methotrexate Disodium
INJECTION, POWDER, LYOPHILIZED, For Solution	1	Methotrexate
TABLET, Film Coated	1	Trexall

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals