NDC 70771-1058 – Methotrexate

Methotrexate 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1058

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207812
Marketed since
February 9, 2017
Listing expires
December 31, 2026
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (6)

Package NDCDescriptionSince
70771-1058-01000 TABLET in 1 BOTTLE (70771-1058-0)Feb 9, 2017
70771-1058-1100 TABLET in 1 BOTTLE (70771-1058-1)Feb 9, 2017
70771-1058-336 TABLET in 1 BOTTLE (70771-1058-3)Feb 9, 2017
70771-1058-5500 TABLET in 1 BOTTLE (70771-1058-5)Feb 9, 2017
70771-1058-7100 BLISTER PACK in 1 CARTON (70771-1058-7) / 1 TABLET in 1 BLISTER PACK (70771-1058-2)Feb 9, 2017
70771-1058-990 TABLET in 1 BOTTLE (70771-1058-9)Feb 9, 2017

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