NDC 71205-049 – Allopurinol

Allopurinol 300 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-049

Product details

Brand name
Allopurinol
Generic name
Allopurinol
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203154
Marketed since
April 29, 2015
Listing expires
December 31, 2026
Pharmacologic class
Xanthine Oxidase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Allopurinol →

Package NDC codes (3)

Package NDCDescriptionSince
71205-049-3030 TABLET in 1 BOTTLE (71205-049-30)Jun 1, 2018
71205-049-6060 TABLET in 1 BOTTLE (71205-049-60)Jun 1, 2018
71205-049-9090 TABLET in 1 BOTTLE (71205-049-90)Jun 1, 2018

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