NDC 68071-2997 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-2997

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211820
Marketed since
March 12, 2019
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
68071-2997-330 TABLET in 1 BOTTLE, PLASTIC (68071-2997-3)May 5, 2023
68071-2997-990 TABLET in 1 BOTTLE, PLASTIC (68071-2997-9)May 5, 2023

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