allopurinol

Generic: allopurinol

Labeler: zydus pharmaceuticals (usa) inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allopurinol
Generic Name allopurinol
Labeler zydus pharmaceuticals (usa) inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

allopurinol 200 mg/1

Manufacturer
Zydus Pharmaceuticals (USA) Inc.

Identifiers & Regulatory

Product NDC 70710-2009
Product ID 70710-2009_95c7021b-a1a5-4a7f-aacf-275a64fe8b58
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210117
Listing Expiration 2026-12-31
Marketing Start 2025-06-17

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 707102009
Hyphenated Format 70710-2009

Supplemental Identifiers

RxCUI
197319 197320 245422
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 ANDA210117 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (70710-2009-0)
  • 90 TABLET in 1 BOTTLE (70710-2009-9)
source: ndc

Packages (2)

70710-2009-0 1000 TABLET in 1 BOTTLE (70710-2009-0) 70710-2009-9 90 TABLET in 1 BOTTLE (70710-2009-9)

Ingredients (1)

allopurinol (200 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": "95c7021b-a1a5-4a7f-aacf-275a64fe8b58", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320", "245422"], "spl_set_id": ["8b926e62-3a9c-424a-833a-8169e55a1f15"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70710-2009-0)", "package_ndc": "70710-2009-0", "marketing_start_date": "20250617"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70710-2009-9)", "package_ndc": "70710-2009-9", "marketing_start_date": "20250617"}], "brand_name": "Allopurinol", "product_id": "70710-2009_95c7021b-a1a5-4a7f-aacf-275a64fe8b58", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70710-2009", "generic_name": "Allopurinol", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "200 mg/1"}], "application_number": "ANDA210117", "marketing_category": "ANDA", "marketing_start_date": "20250617", "listing_expiration_date": "20261231"}