NDC 54436-015 – Otrexup

Methotrexate 15 mg/.4mL · Injection, Solution · Subcutaneous

Human Prescription Drug

Product NDC54436-015

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
54436-015-011 SYRINGE in 1 CARTON (54436-015-01) / .4 mL in 1 SYRINGEOct 11, 2013
54436-015-03 sample1 SYRINGE in 1 CARTON (54436-015-03) / .4 mL in 1 SYRINGEOct 11, 2013
54436-015-044 SYRINGE in 1 CARTON (54436-015-04) / .4 mL in 1 SYRINGE (54436-015-02)Oct 11, 2013

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