allopurinol

Generic: allopurinol

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 300 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-517
Product ID 62135-517_4b432cc5-11c8-4450-e063-6394a90a1053
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077353
Listing Expiration 2027-12-31
Marketing Start 2006-05-11

Pharmacologic Class

Established (EPC)
xanthine oxidase inhibitor [epc]
Mechanism of Action
xanthine oxidase inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135517
Hyphenated Format 62135-517

Supplemental Identifiers

RxCUI
197319 197320
UPC
0362135517908 0362135516901
UNII
63CZ7GJN5I
NUI
N0000175698 N0000000206

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name allopurinol (source: ndc)
Generic Name allopurinol (source: ndc)
Application Number ANDA077353 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 300 mg/1
source: ndc
Packaging
  • 300 TABLET in 1 BOTTLE (62135-517-31)
  • 90 TABLET in 1 BOTTLE (62135-517-90)
source: ndc

Packages (2)

62135-517-31 300 TABLET in 1 BOTTLE (62135-517-31) 62135-517-90 90 TABLET in 1 BOTTLE (62135-517-90)

Ingredients (1)

allopurinol (300 mg/1)

Linked Drug Pages (1)

Allopurinol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b432cc5-11c8-4450-e063-6394a90a1053", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0362135517908", "0362135516901"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["cdc3f33b-ff2b-4a84-a820-51a497fdf3d9"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (62135-517-31)", "package_ndc": "62135-517-31", "marketing_start_date": "20230127"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-517-90)", "package_ndc": "62135-517-90", "marketing_start_date": "20230127"}], "brand_name": "Allopurinol", "product_id": "62135-517_4b432cc5-11c8-4450-e063-6394a90a1053", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "62135-517", "generic_name": "Allopurinol", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA077353", "marketing_category": "ANDA", "marketing_start_date": "20060511", "listing_expiration_date": "20271231"}