Allopurinol

Product NDC: 60760-710
11-digit product format: 607600710
Labeler code: 60760
Product ID: 60760-710_42de3b25-692a-eaff-e063-6294a90a0d21
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Allopurinol
Dosage form: TABLET
Route: ORAL
Labeler: ST. MARY'S MEDICAL PARK PHARMACY
Application: ANDA214443
Marketing category: ANDA
Marketing start: 2024-05-01
Substance: ALLOPURINOL
Active strength: 100 mg/1
Pharmacologic classes: Xanthine Oxidase Inhibitor [EPC], Xanthine Oxidase Inhibitors [MoA]
NDC exclude flag: No
Listing certified through: 2026-12-31
Current FDA listing: Yes

openFDA Listing Details

Product ID: 60760-710_42de3b25-692a-eaff-e063-6294a90a0d21
SPL ID: 42de3b25-692a-eaff-e063-6294a90a0d21
Product type: HUMAN PRESCRIPTION DRUG
Finished product: Yes
Brand name base: Allopurinol
Generic name: Allopurinol
Dosage form: TABLET
Route: ORAL
Marketing start: 2024-05-01
Marketing category: ANDA
Application number: ANDA214443
Pharmacologic classes: Xanthine Oxidase Inhibitor [EPC]; Xanthine Oxidase Inhibitors [MoA]
Listing expiration: 2026-12-31

Ingredient	Strength
ALLOPURINOL	100 mg/1

Field	Values
Unii	63CZ7GJN5I
Rxcui	197319
Spl Set Id	42de3b18-a289-e49e-e063-6394a90a89d4
Manufacturer Name	ST. MARY'S MEDICAL PARK PHARMACY

Package NDC	Description	Marketing start	Sample
60760-710-90	90 TABLET in 1 BOTTLE, PLASTIC (60760-710-90)	2025-11-05	No

UNII	Preferred term	Registry number	Matched term
63CZ7GJN5I	ALLOPURINOL	315-30-0	ALLOPURINOL

Package NDC	11-digit format	Description	Units	Marketing start	Sample	Exclude flag	Status
60760-710-90	60760071090	90 TABLET in 1 BOTTLE, PLASTIC (60760-710-90)	90 tablet	2025-11-05	No	No	Historical

Title	Manufacturer	Effective date	Type	Version
Allopurinol	ST. MARY'S MEDICAL PARK PHARMACY	2025-11-05	HUMAN PRESCRIPTION DRUG LABEL	1