NDC 68071-3672 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3672

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214443
Marketed since
May 1, 2024
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (1)

Package NDCDescriptionSince
68071-3672-990 TABLET in 1 BOTTLE (68071-3672-9)Aug 30, 2024

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