Allopurinol

Product NDC
60429-181
11-digit product format
604290181
Labeler code
60429
Product ID
60429-181_7cd6d025-f5d4-07a8-e053-2991aa0a3f51
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Allopurinol
Dosage form
TABLET
Route
ORAL
Labeler
Golden State Medical Supply, Inc.
Application
ANDA071587
Marketing category
ANDA
Marketing start
2015-02-09
Marketing end
0000-00-00
Substance
ALLOPURINOL
Active strength
300 mg/1
Pharmacologic classes
Xanthine Oxidase Inhibitor [EPC],Xanthine Oxidase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ee55bab-4ea8-ac26-c688-380cfbcd5c03Product name720260127
de89a493-168f-43fa-9852-1f15e00dbb17Product name120221110
4a2a34d6-1853-423b-9e0c-360370b95802Product name120171006

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60429-181-01EA - Each60429-1811b2b97fb-652f-4119-b2a1-cf674d610dd912015-05-05
60429-181-05EA - Each60429-1812c8a6011-2853-4dac-8749-d84dd92624ed12015-05-05
60429-181-90EA - Each60429-18101201a69-9da0-47f0-8bc0-66e24919f90c12015-05-05

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197320allopurinol 300 MG Oral TabletPSNeeb51b29-5b46-495d-9c86-8afd710404bc3
197320allopurinol 300 MG Oral TabletSCDeeb51b29-5b46-495d-9c86-8afd710404bc3