NDC 68382-775 – Methotrexate

Methotrexate 2.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68382-775

Product details

Brand name
Methotrexate
Generic name
Methotrexate
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207812
Marketed since
February 9, 2017
Listing expires
December 31, 2027
Pharmacologic class
Folate Analog Metabolic Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Methotrexate →

Package NDC codes (6)

Package NDCDescriptionSince
68382-775-01100 TABLET in 1 BOTTLE (68382-775-01)Feb 9, 2017
68382-775-05500 TABLET in 1 BOTTLE (68382-775-05)Feb 9, 2017
68382-775-101000 TABLET in 1 BOTTLE (68382-775-10)Feb 9, 2017
68382-775-1690 TABLET in 1 BOTTLE (68382-775-16)Feb 9, 2017
68382-775-6036 TABLET in 1 BOTTLE (68382-775-60)Feb 9, 2017
68382-775-77100 BLISTER PACK in 1 CARTON (68382-775-77) / 1 TABLET in 1 BLISTER PACKFeb 9, 2017

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