allopurinol

Generic: allopurinol

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-693
Product ID 23155-693_43518352-e2b6-4133-97fc-860d3eeea074
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204467
Marketing Start 2020-09-22
Marketing End 2029-10-31

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 23155693
Hyphenated Format 23155-693

Supplemental Identifiers

RxCUI
197319 197320
UPC
0323155693010 0323155694017
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 ANDA204467 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-693-01)
  • 1000 TABLET in 1 BOTTLE (23155-693-10)
source: ndc

Packages (2)

23155-693-01 100 TABLET in 1 BOTTLE (23155-693-01) 23155-693-10 1000 TABLET in 1 BOTTLE (23155-693-10)

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": "43518352-e2b6-4133-97fc-860d3eeea074", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0323155693010", "0323155694017"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["ad6950d4-2cdd-44ac-9b8a-120716460e70"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-693-01)", "package_ndc": "23155-693-01", "marketing_end_date": "20270930", "marketing_start_date": "20200922"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-693-10)", "package_ndc": "23155-693-10", "marketing_end_date": "20290331", "marketing_start_date": "20200922"}], "brand_name": "Allopurinol", "product_id": "23155-693_43518352-e2b6-4133-97fc-860d3eeea074", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "23155-693", "generic_name": "Allopurinol", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_end_date": "20291031", "marketing_start_date": "20200922"}