NDC 46708-730 – Methotrexate

Methotrexate Sodium 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC46708-730

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA217552
Marketed since
June 4, 2024
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (2)

Package NDCDescriptionSince
46708-730-31100 TABLET in 1 BOTTLE (46708-730-31)Jun 4, 2024
46708-730-3636 TABLET in 1 BOTTLE (46708-730-36)Jun 4, 2024

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