NDC 54436-017 – Otrexup

Methotrexate 17.5 mg/.4mL · Injection, Solution · Subcutaneous

Human Prescription Drug

Product NDC54436-017

Product details

Brand name
Otrexup
Generic name
methotrexate
Labeler
Antares Pharma, Inc.
Dosage form
Injection, Solution
Route
Subcutaneous
Marketing category
NDA · NDA204824
Marketed since
October 11, 2013
Marketing end
April 30, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Otrexup →

Package NDC codes (3)

Package NDCDescriptionSince
54436-017-011 SYRINGE in 1 CARTON (54436-017-01) / .4 mL in 1 SYRINGEMar 24, 2016
54436-017-03 sample1 SYRINGE in 1 CARTON (54436-017-03) / .4 mL in 1 SYRINGEMar 24, 2016
54436-017-044 SYRINGE in 1 CARTON (54436-017-04) / .4 mL in 1 SYRINGE (54436-017-02)Mar 24, 2016

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