NDC 0378-0137 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0378-0137

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA018659
Marketed since
October 24, 1986
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (2)

Package NDCDescriptionSince
0378-0137-01100 TABLET in 1 BOTTLE (0378-0137-01)Oct 24, 1986
0378-0137-101000 TABLET in 1 BOTTLE (0378-0137-10)Oct 24, 1986

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