NDC 51285-369 – Trexall

Methotrexate Sodium 15 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51285-369

Product details

Brand name
Trexall
Generic name
Methotrexate
Labeler
Teva Women's Health LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA040385
Marketed since
May 3, 2001
Listing expires
December 31, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Trexall →

Package NDC codes (1)

Package NDCDescriptionSince
51285-369-0130 TABLET, FILM COATED in 1 BOTTLE (51285-369-01)May 3, 2001

Other Trexall products