allopurinol

Generic: allopurinol

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-935
Product ID 43063-935_415e8afc-cefe-973f-e063-6394a90a4167
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 43063935
Hyphenated Format 43063-935

Supplemental Identifiers

RxCUI
197319
UPC
0343063935019
UNII
63CZ7GJN5I
NUI
N0000175698 N0000000206

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 (43063-935-01)
source: ndc

Packages (1)

43063-935-01 100 TABLET in 1 BOTTLE, PLASTIC (43063-935-01)

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": "415e8afc-cefe-973f-e063-6394a90a4167", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0343063935019"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["f130c9c0-45d8-42bc-a040-04bb077671f8"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (43063-935-01)", "package_ndc": "43063-935-01", "marketing_start_date": "20190129"}], "brand_name": "Allopurinol", "product_id": "43063-935_415e8afc-cefe-973f-e063-6394a90a4167", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "43063-935", "generic_name": "Allopurinol", "labeler_name": "PD-Rx Pharmaceuticals, 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"}