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NDC 70199-0031-99 Zyloprim 100 mg/1 Details

Zyloprim 100 mg/1

Zyloprim is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Casper Pharma LLC. The primary component is ALLOPURINOL.

MedlinePlus Drug Summary

Allopurinol is used to treat gout (a type of arthritis in which uric acid, a naturally occurring substance in the body, builds up in the joints and causes sudden attacks of redness, swelling, pain, and heat in one or more joints). Allopurinol is also used to treat high levels of uric acid that builds up in the blood as tumors break down in people with certain types of cancer who are being treated with chemotherapy medications. It is also used to treat kidney stones that have come back in people who have high levels of uric acid in their urine. Allopurinol is in a class of medications called xanthine oxidase inhibitors. It works by reducing the production of uric acid in the body. High levels of uric acid may cause gout attacks or kidney stones. Allopurinol is used to prevent gout attacks, not to treat them once they occur.

Related Packages: 70199-0031-99
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Allopurinol

Product Information

NDC	70199-0031
Product ID	70199-031_a7d28982-23c9-4e82-b73c-7b2cd0079d0e
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Zyloprim
Proprietary Name Suffix	n/a
Non-Proprietary Name	allopurinol
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	ALLOPURINOL
Labeler Name	Casper Pharma LLC
Pharmaceutical Class	Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
DEA Schedule	n/a
Marketing Category	NDA
Application Number	NDA016084
Listing Certified Through	2024-12-31

Package

NDC 70199-0031-99 (70199003199)

Pricing Information	N/A
NDC Package Code	70199-031-99
Billing NDC	70199003199
Package	1000 TABLET in 1 BOTTLE (70199-031-99)
Marketing Start Date	2023-09-21
NDC Exclude Flag	N