allopurinol

Generic: allopurinol

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler redpharm drug
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 100 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-1897
Product ID 67296-1897_2c630c05-3e4e-fe4c-e063-6394a90a07cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA204467
Listing Expiration 2026-12-31
Marketing Start 2020-09-22

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 672961897
Hyphenated Format 67296-1897

Supplemental Identifiers

RxCUI
197319
UPC
0323155693102 0323155693010 0323155694055 0323155694017
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 ANDA204467 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (67296-1897-3)
source: ndc

Packages (1)

67296-1897-3 30 TABLET in 1 BOTTLE (67296-1897-3)

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": "2c630c05-3e4e-fe4c-e063-6394a90a07cd", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0323155693102", "0323155693010", "0323155694055", "0323155694017"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["0a22fa72-c363-4e96-e063-6394a90a48aa"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-1897-3)", "package_ndc": "67296-1897-3", "marketing_start_date": "20200922"}], "brand_name": "Allopurinol", "product_id": "67296-1897_2c630c05-3e4e-fe4c-e063-6394a90a07cd", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "67296-1897", "generic_name": "Allopurinol", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20200922", "listing_expiration_date": "20261231"}