NDC 46708-711 – Methotrexate

Methotrexate Sodium 25 mg/mL · Injection, Solution · Intramuscular, Intravenous, Subcutaneous

Human Prescription Drug

Product NDC46708-711

Product details

Brand name
Methotrexate
Generic name
methotrexate
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous, Subcutaneous
Marketing category
ANDA · ANDA220225
Marketed since
April 15, 2026
Listing expires
December 31, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (1)

Package NDCDescriptionSince
46708-711-055 VIAL, MULTI-DOSE in 1 CARTON (46708-711-05) / 2 mL in 1 VIAL, MULTI-DOSE (46708-711-01)Apr 15, 2026

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