NDC 71335-9641 – Allopurinol

Allopurinol 100 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9641

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211820
Marketed since
March 12, 2019
Listing expires
December 31, 2027
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (6)

Package NDCDescriptionSince
71335-9641-1100 TABLET in 1 BOTTLE, PLASTIC (71335-9641-1)Sep 6, 2023
71335-9641-230 TABLET in 1 BOTTLE, PLASTIC (71335-9641-2)Feb 14, 2023
71335-9641-360 TABLET in 1 BOTTLE, PLASTIC (71335-9641-3)Dec 11, 2023
71335-9641-4120 TABLET in 1 BOTTLE, PLASTIC (71335-9641-4)Apr 15, 2026
71335-9641-520 TABLET in 1 BOTTLE, PLASTIC (71335-9641-5)Apr 15, 2026
71335-9641-690 TABLET in 1 BOTTLE, PLASTIC (71335-9641-6)Mar 3, 2023

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