allopurinol

Generic: allopurinol

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 53489-156
Product ID 53489-156_11692a2c-370e-2685-e063-6394a90a764a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071450
Listing Expiration 2026-12-31
Marketing Start 1987-01-09

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 53489156
Hyphenated Format 53489-156

Supplemental Identifiers

RxCUI
197319 197320
UPC
0353489157018
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 ANDA071450 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (53489-156-01)
  • 50 TABLET in 1 BOTTLE, PLASTIC (53489-156-02)
  • 500 TABLET in 1 BOTTLE, PLASTIC (53489-156-05)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (53489-156-10)
source: ndc

Packages (4)

53489-156-01 100 TABLET in 1 BOTTLE, PLASTIC (53489-156-01) 53489-156-02 50 TABLET in 1 BOTTLE, PLASTIC (53489-156-02) 53489-156-05 500 TABLET in 1 BOTTLE, PLASTIC (53489-156-05) 53489-156-10 1000 TABLET in 1 BOTTLE, PLASTIC (53489-156-10)

Ingredients (1)

allopurinol (100 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": "11692a2c-370e-2685-e063-6394a90a764a", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0353489157018"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["fd8f8b8b-f25e-46e9-969a-65363b66e09b"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (53489-156-01)", "package_ndc": "53489-156-01", "marketing_start_date": "19870109"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE, PLASTIC (53489-156-02)", "package_ndc": "53489-156-02", "marketing_start_date": "19870109"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (53489-156-05)", "package_ndc": "53489-156-05", "marketing_start_date": "19870109"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (53489-156-10)", "package_ndc": "53489-156-10", "marketing_start_date": "19870109"}], "brand_name": "Allopurinol", "product_id": "53489-156_11692a2c-370e-2685-e063-6394a90a764a", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "53489-156", "generic_name": "Allopurinol", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA071450", "marketing_category": "ANDA", "marketing_start_date": "19870109", "listing_expiration_date": "20261231"}